Canonical Allele Identifier: CA2779774146

Gene: FGFR1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.38416061_38416062insATCC , CM000670.2:g.38416061_38416062insATCC	GRCh38
NC_000008.10:g.38273579_38273580insATCC , CM000670.1:g.38273579_38273580insATCC	GRCh37
NC_000008.9:g.38392736_38392737insATCC	NCBI36
NG_007729.1:g.57775_57776insATGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703405.1:c.1664_1665insATGG
ENST00000341462.9:c.1652_1653insATGG
ENST00000425967.8:c.1652_1653insATGG
ENST00000524528.2:n.2557_2558insATGG
ENST00000682398.1:n.486_487insATGG
ENST00000683132.1:n.354_355insATGG
ENST00000683765.1:c.1844_1845insATGG
ENST00000683815.1:c.1652_1653insATGG
ENST00000683948.1:n.2352_2353insATGG
ENST00000684654.1:c.1385_1386insATGG
ENST00000447712.7:c.1664_1665insATGG
ENST00000649678.1:c.1652_1653insATGG
ENST00000674189.1:c.*1310_*1311insATGG
ENST00000674380.1:c.*1631_*1632insATGG
ENST00000674474.1:n.3158_3159insATGG
ENST00000326324.10:c.1391_1392insATGG
ENST00000335922.9:c.1634_1635insATGG
ENST00000341462.8:c.*714_*715insATGG
ENST00000356207.9:c.1397_1398insATGG
ENST00000397091.9:c.1658_1659insATGG
ENST00000397103.5:c.1397_1398insATGG
ENST00000397108.8:c.1658_1659insATGG
ENST00000397113.6:c.1658_1659insATGG
ENST00000425967.7:c.1757_1758insATGG
ENST00000447712.6:c.1664_1665insATGG
ENST00000487647.5:c.1541_1542insATGG
ENST00000526570.5:n.3943_3944insATGG
ENST00000527114.5:n.1186_1187insATGG
ENST00000532791.5:c.1658_1659insATGG
ENST00000533619.5:n.210_211insATGG
ENST00000619564.3:c.*559_*560insATGG
NM_001174063.1:c.1658_1659insATGG
NM_001174064.1:c.1634_1635insATGG
NM_001174065.1:c.1658_1659insATGG
NM_001174066.1:c.1397_1398insATGG
NM_001174067.1:c.1757_1758insATGG
NM_015850.3:c.1658_1659insATGG
NM_023105.2:c.1397_1398insATGG
NM_023106.2:c.1391_1392insATGG
NM_023110.2:c.1664_1665insATGG
XM_006716303.2:c.1664_1665insATGG
XM_006716304.1:c.1664_1665insATGG
XM_006716305.2:c.1664_1665insATGG
XM_006716306.2:c.1658_1659insATGG
XM_006716307.1:c.1658_1659insATGG
XM_006716309.2:c.1640_1641insATGG
XM_006716310.2:c.1397_1398insATGG
XM_006716311.1:c.1397_1398insATGG
XM_006716312.1:c.1397_1398insATGG
XM_006716313.2:c.1391_1392insATGG
XM_006716314.1:c.1391_1392insATGG
XM_011544443.1:c.1763_1764insATGG
XM_011544444.1:c.1757_1758insATGG
XM_011544445.1:c.1757_1758insATGG
XM_011544446.1:c.1763_1764insATGG
XM_011544447.1:c.1757_1758insATGG
XM_011544448.1:c.1496_1497insATGG
XM_011544449.1:c.1490_1491insATGG
XM_011544450.1:c.1490_1491insATGG
XM_011544451.1:c.1373_1374insATGG
NM_001354367.1:c.1658_1659insATGG
NM_001354368.1:c.1385_1386insATGG
NM_001354369.1:c.1652_1653insATGG
NM_001354370.1:c.1391_1392insATGG
XM_006716303.3:c.1664_1665insATGG
XM_006716310.3:c.1397_1398insATGG
XM_006716312.2:c.1397_1398insATGG
XM_006716314.2:c.1391_1392insATGG
XM_011544443.2:c.1763_1764insATGG
XM_011544445.2:c.1757_1758insATGG
XM_011544446.2:c.1763_1764insATGG
XM_011544447.2:c.1757_1758insATGG
XM_011544450.2:c.1490_1491insATGG
XM_017013219.1:c.1751_1752insATGG
XM_017013220.1:c.1751_1752insATGG
XM_017013221.1:c.1664_1665insATGG
XM_017013222.2:c.1658_1659insATGG
XM_017013224.2:c.1652_1653insATGG
XM_017013225.2:c.1652_1653insATGG
XM_017013226.1:c.1490_1491insATGG
XM_017013227.1:c.1484_1485insATGG
XM_017013229.2:c.692_693insATGG
XM_017013230.1:c.692_693insATGG
XM_024447097.1:c.1640_1641insATGG
XR_001745495.1:n.1912_1913insATGG
XR_001745496.1:n.1912_1913insATGG
NM_001174063.2:c.1658_1659insATGG
NM_001174064.2:c.1634_1635insATGG
NM_001174065.2:c.1658_1659insATGG
NM_001174066.2:c.1397_1398insATGG
NM_001354368.2:c.1385_1386insATGG
NM_015850.4:c.1658_1659insATGG
NM_023105.3:c.1397_1398insATGG
NM_023106.3:c.1391_1392insATGG
NM_023110.3:c.1664_1665insATGG
NM_001174067.2:c.1757_1758insATGG
NM_001354367.2:c.1658_1659insATGG
NM_001354369.2:c.1652_1653insATGG
NM_001354370.2:c.1391_1392insATGG