Canonical Allele Identifier: CA10630949
Gene: FGFR1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 362864
dbSNP Id: rs13317

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38411996T>C , CM000670.2:g.38411996T>C GRCh38
NC_000008.10:g.38269514T>C , CM000670.1:g.38269514T>C GRCh37
NC_000008.9:g.38388671T>C NCBI36
NG_007729.1:g.61839A>G

Transcript Alleles

HGVS Amino-acid change
NM_001174063.1:c.*1632A>G VV NP_001167534.1:p.=
NM_001174064.1:c.*1632A>G VV NP_001167535.1:p.=
NM_001174065.1:c.*1632A>G VV NP_001167536.1:p.=
NM_001174066.1:c.*1632A>G VV NP_001167537.1:p.=
NM_001174067.1:c.*1632A>G VV NP_001167538.1:p.=
NM_015850.3:c.*1632A>G VV NP_056934.2:p.=
NM_023105.2:c.*1632A>G VV NP_075593.1:p.=
NM_023106.2:c.*1632A>G VV NP_075594.1:p.=
NM_023110.2:c.*1632A>G VV NP_075598.2:p.=
XM_006716303.2:c.*393A>G XP_006716366.1:p.=
XM_006716304.1:c.*393A>G XP_006716367.1:p.=
XM_006716305.2:c.*393A>G XP_006716368.1:p.=
XM_006716306.2:c.*393A>G XP_006716369.1:p.=
XM_006716307.1:c.*393A>G XP_006716370.1:p.=
XM_006716309.2:c.*393A>G XP_006716372.1:p.=
XM_006716310.2:c.*393A>G XP_006716373.1:p.=
XM_006716311.1:c.*393A>G XP_006716374.1:p.=
XM_006716312.1:c.*393A>G XP_006716375.1:p.=
XM_006716313.2:c.*393A>G XP_006716376.1:p.=
XM_006716314.1:c.*393A>G XP_006716377.1:p.=
XM_011544443.1:c.*393A>G XP_011542745.1:p.=
XM_011544444.1:c.*393A>G XP_011542746.1:p.=
XM_011544445.1:c.*393A>G XP_011542747.1:p.=
XM_011544448.1:c.*393A>G XP_011542750.1:p.=
XM_011544449.1:c.*393A>G XP_011542751.1:p.=
XM_011544451.1:c.*393A>G XP_011542753.1:p.=
NM_001354367.1:c.*393A>G VV NP_001341296.1:p.=
NM_001354368.1:c.*1632A>G VV NP_001341297.1:p.=
NM_001354369.1:c.*393A>G VV NP_001341298.1:p.=
NM_001354370.1:c.*393A>G VV NP_001341299.1:p.=
XM_006716303.3:c.*393A>G XP_006716366.1:p.=
XM_006716310.3:c.*393A>G XP_006716373.1:p.=
XM_006716312.2:c.*393A>G XP_006716375.1:p.=
XM_006716314.2:c.*393A>G XP_006716377.1:p.=
XM_011544443.2:c.*393A>G XP_011542745.1:p.=
XM_011544445.2:c.*393A>G XP_011542747.1:p.=
XM_011544446.2:c.*1632A>G XP_011542748.1:p.=
XM_011544447.2:c.*1632A>G XP_011542749.1:p.=
XM_011544450.2:c.*1632A>G XP_011542752.1:p.=
XM_017013219.1:c.*393A>G XP_016868708.1:p.=
XM_017013220.1:c.*1632A>G XP_016868709.1:p.=
XM_017013221.1:c.*393A>G XP_016868710.1:p.=
XM_017013222.2:c.*393A>G XP_016868711.1:p.=
XM_017013224.2:c.*1632A>G XP_016868713.1:p.=
XM_017013225.2:c.*1632A>G XP_016868714.1:p.=
XM_017013226.1:c.*1632A>G XP_016868715.1:p.=
XM_017013227.1:c.*1632A>G XP_016868716.1:p.=
XM_017013229.2:c.*393A>G XP_016868718.1:p.=
XM_017013230.1:c.*1632A>G XP_016868719.1:p.=
XM_024447097.1:c.*393A>G XP_024302865.1:p.=
XR_001745496.1:n.3165A>G
ENST00000341462.8:c.*3151A>G ENSP00000340636.6:p.=
ENST00000397091.9:c.*1632A>G ENSP00000380280.5:p.=
ENST00000425967.7:c.*1632A>G ENSP00000393312.3:p.=
ENST00000447712.6:c.*1632A>G ENSP00000400162.2:p.=
ENST00000532791.5:c.*1632A>G ENSP00000432972.1:p.=
ENST00000619564.3:c.*2996A>G ENSP00000484553.1:p.=