Canonical Allele Identifier: CA2779773780

Gene: FGFR1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.38414024_38414151del , CM000670.2:g.38414024_38414151del	GRCh38
NC_000008.10:g.38271542_38271669del , CM000670.1:g.38271542_38271669del	GRCh37
NC_000008.9:g.38390699_38390826del	NCBI36
NG_007729.1:g.59687_59814del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703405.1:c.2186+4_2189del
ENST00000341462.9:c.2174+4_2177del
ENST00000425967.8:c.2174+4_2177del
ENST00000524528.2:n.3079+4_3082del
ENST00000682398.1:n.1426+4_1429del
ENST00000683132.1:n.876+4_879del
ENST00000683765.1:c.2366+4_2369del
ENST00000683815.1:c.2174+4_2177del
ENST00000683948.1:n.2874+4_2877del
ENST00000684654.1:c.1907+4_1910del
ENST00000447712.7:c.2186+4_2189del
ENST00000649678.1:c.2174+4_2177del
ENST00000674189.1:c.*1832+4_*1835del
ENST00000674380.1:c.*2153+4_*2156del
ENST00000674474.1:n.3680+4_3683del
ENST00000326324.10:c.1913+4_1916del
ENST00000335922.9:c.2156+4_2159del
ENST00000341462.8:c.*1236+4_*1239del
ENST00000356207.9:c.1919+4_1922del
ENST00000397091.9:c.2180+4_2183del
ENST00000397103.5:c.1919+4_1922del
ENST00000397108.8:c.2180+4_2183del
ENST00000397113.6:c.2180+4_2183del
ENST00000425967.7:c.2279+4_2282del
ENST00000447712.6:c.2186+4_2189del
ENST00000526570.5:n.4465+4_4468del
ENST00000531196.5:c.386+4_400del
ENST00000532791.5:c.2180+4_2183del
ENST00000619564.3:c.*1081+4_*1084del
NM_001174063.1:c.2180+4_2183del
NM_001174064.1:c.2156+4_2159del
NM_001174065.1:c.2180+4_2183del
NM_001174066.1:c.1919+4_1922del
NM_001174067.1:c.2279+4_2282del
NM_015850.3:c.2180+4_2183del
NM_023105.2:c.1919+4_1922del
NM_023106.2:c.1913+4_1916del
NM_023110.2:c.2186+4_2189del
XM_006716303.2:c.2186+4_2189del
XM_006716304.1:c.2186+4_2189del
XM_006716305.2:c.2186+4_2189del
XM_006716306.2:c.2180+4_2183del
XM_006716307.1:c.2180+4_2183del
XM_006716309.2:c.2162+4_2165del
XM_006716310.2:c.1919+4_1922del
XM_006716311.1:c.1919+4_1922del
XM_006716312.1:c.1919+4_1922del
XM_006716313.2:c.1913+4_1916del
XM_006716314.1:c.1913+4_1916del
XM_011544443.1:c.2285+4_2288del
XM_011544444.1:c.2279+4_2282del
XM_011544445.1:c.2279+4_2282del
XM_011544446.1:c.2285+4_2288del
XM_011544447.1:c.2279+4_2282del
XM_011544448.1:c.2018+4_2021del
XM_011544449.1:c.2012+4_2015del
XM_011544450.1:c.2012+4_2015del
XM_011544451.1:c.1895+4_1898del
NM_001354367.1:c.2180+4_2183del
NM_001354368.1:c.1907+4_1910del
NM_001354369.1:c.2174+4_2177del
NM_001354370.1:c.1913+4_1916del
XM_006716303.3:c.2186+4_2189del
XM_006716310.3:c.1919+4_1922del
XM_006716312.2:c.1919+4_1922del
XM_006716314.2:c.1913+4_1916del
XM_011544443.2:c.2285+4_2288del
XM_011544445.2:c.2279+4_2282del
XM_011544446.2:c.2285+4_2288del
XM_011544447.2:c.2279+4_2282del
XM_011544450.2:c.2012+4_2015del
XM_017013219.1:c.2273+4_2276del
XM_017013220.1:c.2273+4_2276del
XM_017013221.1:c.2186+4_2189del
XM_017013222.2:c.2180+4_2183del
XM_017013224.2:c.2174+4_2177del
XM_017013225.2:c.2174+4_2177del
XM_017013226.1:c.2012+4_2015del
XM_017013227.1:c.2006+4_2009del
XM_017013229.2:c.1214+4_1217del
XM_017013230.1:c.1214+4_1217del
XM_024447097.1:c.2162+4_2165del
XR_001745495.1:n.2459+4_2462del
XR_001745496.1:n.2459+4_2462del
NM_001174063.2:c.2180+4_2183del
NM_001174064.2:c.2156+4_2159del
NM_001174065.2:c.2180+4_2183del
NM_001174066.2:c.1919+4_1922del
NM_001354368.2:c.1907+4_1910del
NM_015850.4:c.2180+4_2183del
NM_023105.3:c.1919+4_1922del
NM_023106.3:c.1913+4_1916del
NM_023110.3:c.2186+4_2189del
NM_001174067.2:c.2279+4_2282del
NM_001354367.2:c.2180+4_2183del
NM_001354369.2:c.2174+4_2177del
NM_001354370.2:c.1913+4_1916del