Canonical Allele Identifier: CA2740094994
Gene: FGFR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2943353
ClinVar RCV Id: RCV003800471

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38415904_38415933del , CM000670.2:g.38415904_38415933del GRCh38
NC_000008.10:g.38273422_38273451del , CM000670.1:g.38273422_38273451del GRCh37
NC_000008.9:g.38392579_38392608del NCBI36
NG_007729.1:g.57902_57931del

Transcript Alleles

HGVS Amino-acid change
ENST00000703405.1:c.1791_1820del ENSP00000515291.1:p.Lys598_Val607del
ENST00000341462.9:c.1779_1808del ENSP00000340636.7:p.Lys594_Val603del
ENST00000425967.8:c.1779_1808del ENSP00000393312.4:p.Lys594_Val603del
ENST00000524528.2:n.2684_2713del
ENST00000682398.1:n.613_642del
ENST00000683132.1:n.481_510del
ENST00000683765.1:c.1971_2000del ENSP00000507039.1:p.Lys658_Val667del
ENST00000683815.1:c.1779_1808del ENSP00000507997.1:p.Lys594_Val603del
ENST00000683948.1:n.2479_2508del
ENST00000684654.1:c.1512_1541del ENSP00000507205.1:p.Lys505_Val514del
ENST00000447712.7:c.1791_1820del MANE Select ENSP00000400162.2:p.Lys598_Val607del
ENST00000649678.1:c.1779_1808del ENSP00000497266.1:p.Lys594_Val603del
ENST00000674189.1:c.*1437_*1466del ENSP00000501345.1:n.*1437_*1466del
ENST00000674380.1:c.*1758_*1787del ENSP00000501514.1:n.*1758_*1787del
ENST00000674474.1:n.3285_3314del
ENST00000326324.10:c.1518_1547del ENSP00000327229.6:p.Lys507_Val516del
ENST00000335922.9:c.1761_1790del ENSP00000337247.5:p.Lys588_Val597del
ENST00000341462.8:c.*841_*870del ENSP00000340636.6:n.*841_*870del
ENST00000356207.9:c.1524_1553del ENSP00000348537.5:p.Lys509_Val518del
ENST00000397091.9:c.1785_1814del ENSP00000380280.5:p.Lys596_Val605del
ENST00000397103.5:c.1524_1553del ENSP00000380292.1:p.Lys509_Val518del
ENST00000397108.8:c.1785_1814del ENSP00000380297.4:p.Lys596_Val605del
ENST00000397113.6:c.1785_1814del ENSP00000380302.2:p.Lys596_Val605del
ENST00000425967.7:c.1884_1913del ENSP00000393312.3:p.Lys629_Val638del
ENST00000447712.6:c.1791_1820del ENSP00000400162.2:p.Lys598_Val607del
ENST00000526570.5:n.4070_4099del
ENST00000527114.5:n.1313_1342del
ENST00000532791.5:c.1785_1814del ENSP00000432972.1:p.Lys596_Val605del
ENST00000533619.5:n.337_366del
ENST00000619564.3:c.*686_*715del ENSP00000484553.1:n.*686_*715del
NM_001174063.1:c.1785_1814del NP_001167534.1:p.Lys596_Val605del
NM_001174064.1:c.1761_1790del NP_001167535.1:p.Lys588_Val597del
NM_001174065.1:c.1785_1814del NP_001167536.1:p.Lys596_Val605del
NM_001174066.1:c.1524_1553del NP_001167537.1:p.Lys509_Val518del
NM_001174067.1:c.1884_1913del NP_001167538.1:p.Lys629_Val638del
NM_015850.3:c.1785_1814del NP_056934.2:p.Lys596_Val605del
NM_023105.2:c.1524_1553del NP_075593.1:p.Lys509_Val518del
NM_023106.2:c.1518_1547del NP_075594.1:p.Lys507_Val516del
NM_023110.2:c.1791_1820del NP_075598.2:p.Lys598_Val607del
XM_006716303.2:c.1791_1820del XP_006716366.1:p.Lys598_Val607del
XM_006716304.1:c.1791_1820del XP_006716367.1:p.Lys598_Val607del
XM_006716305.2:c.1791_1820del XP_006716368.1:p.Lys598_Val607del
XM_006716306.2:c.1785_1814del XP_006716369.1:p.Lys596_Val605del
XM_006716307.1:c.1785_1814del XP_006716370.1:p.Lys596_Val605del
XM_006716309.2:c.1767_1796del XP_006716372.1:p.Lys590_Val599del
XM_006716310.2:c.1524_1553del XP_006716373.1:p.Lys509_Val518del
XM_006716311.1:c.1524_1553del XP_006716374.1:p.Lys509_Val518del
XM_006716312.1:c.1524_1553del XP_006716375.1:p.Lys509_Val518del
XM_006716313.2:c.1518_1547del XP_006716376.1:p.Lys507_Val516del
XM_006716314.1:c.1518_1547del XP_006716377.1:p.Lys507_Val516del
XM_011544443.1:c.1890_1919del XP_011542745.1:p.Lys631_Val640del
XM_011544444.1:c.1884_1913del XP_011542746.1:p.Lys629_Val638del
XM_011544445.1:c.1884_1913del XP_011542747.1:p.Lys629_Val638del
XM_011544446.1:c.1890_1919del XP_011542748.1:p.Lys631_Val640del
XM_011544447.1:c.1884_1913del XP_011542749.1:p.Lys629_Val638del
XM_011544448.1:c.1623_1652del XP_011542750.1:p.Lys542_Val551del
XM_011544449.1:c.1617_1646del XP_011542751.1:p.Lys540_Val549del
XM_011544450.1:c.1617_1646del XP_011542752.1:p.Lys540_Val549del
XM_011544451.1:c.1500_1529del XP_011542753.1:p.Lys501_Val510del
NM_001354367.1:c.1785_1814del NP_001341296.1:p.Lys596_Val605del
NM_001354368.1:c.1512_1541del NP_001341297.1:p.Lys505_Val514del
NM_001354369.1:c.1779_1808del NP_001341298.1:p.Lys594_Val603del
NM_001354370.1:c.1518_1547del NP_001341299.1:p.Lys507_Val516del
XM_006716303.3:c.1791_1820del XP_006716366.1:p.Lys598_Val607del
XM_006716310.3:c.1524_1553del XP_006716373.1:p.Lys509_Val518del
XM_006716312.2:c.1524_1553del XP_006716375.1:p.Lys509_Val518del
XM_006716314.2:c.1518_1547del XP_006716377.1:p.Lys507_Val516del
XM_011544443.2:c.1890_1919del XP_011542745.1:p.Lys631_Val640del
XM_011544445.2:c.1884_1913del XP_011542747.1:p.Lys629_Val638del
XM_011544446.2:c.1890_1919del XP_011542748.1:p.Lys631_Val640del
XM_011544447.2:c.1884_1913del XP_011542749.1:p.Lys629_Val638del
XM_011544450.2:c.1617_1646del XP_011542752.1:p.Lys540_Val549del
XM_017013219.1:c.1878_1907del XP_016868708.1:p.Lys627_Val636del
XM_017013220.1:c.1878_1907del XP_016868709.1:p.Lys627_Val636del
XM_017013221.1:c.1791_1820del XP_016868710.1:p.Lys598_Val607del
XM_017013222.2:c.1785_1814del XP_016868711.1:p.Lys596_Val605del
XM_017013224.2:c.1779_1808del XP_016868713.1:p.Lys594_Val603del
XM_017013225.2:c.1779_1808del XP_016868714.1:p.Lys594_Val603del
XM_017013226.1:c.1617_1646del XP_016868715.1:p.Lys540_Val549del
XM_017013227.1:c.1611_1640del XP_016868716.1:p.Lys538_Val547del
XM_017013229.2:c.819_848del XP_016868718.1:p.Lys274_Val283del
XM_017013230.1:c.819_848del XP_016868719.1:p.Lys274_Val283del
XM_024447097.1:c.1767_1796del XP_024302865.1:p.Lys590_Val599del
XR_001745495.1:n.2039_2068del
XR_001745496.1:n.2039_2068del
NM_001174063.2:c.1785_1814del NP_001167534.1:p.Lys596_Val605del
NM_001174064.2:c.1761_1790del NP_001167535.1:p.Lys588_Val597del
NM_001174065.2:c.1785_1814del NP_001167536.1:p.Lys596_Val605del
NM_001174066.2:c.1524_1553del NP_001167537.1:p.Lys509_Val518del
NM_001354368.2:c.1512_1541del NP_001341297.1:p.Lys505_Val514del
NM_015850.4:c.1785_1814del NP_056934.2:p.Lys596_Val605del
NM_023105.3:c.1524_1553del NP_075593.1:p.Lys509_Val518del
NM_023106.3:c.1518_1547del NP_075594.1:p.Lys507_Val516del
NM_023110.3:c.1791_1820del MANE Select NP_075598.2:p.Lys598_Val607del
NM_001174067.2:c.1884_1913del NP_001167538.1:p.Lys629_Val638del
NM_001354367.2:c.1785_1814del NP_001341296.1:p.Lys596_Val605del
NM_001354369.2:c.1779_1808del NP_001341298.1:p.Lys594_Val603del
NM_001354370.2:c.1518_1547del NP_001341299.1:p.Lys507_Val516del