Canonical Allele Identifier: CA4718544

Gene: FGFR1

Linked Data

• dbSNP Id: rs762987116
• ExAC: 8:38279376 C / G
• gnomAD v4: 8-38421858-C-G
• MyVariant Identifiers: chr8:g.38279376C>G (hg19) ; chr8:g.38421858C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.38421858C>G , CM000670.2:g.38421858C>G	GRCh38
NC_000008.10:g.38279376C>G , CM000670.1:g.38279376C>G	GRCh37
NC_000008.9:g.38398533C>G	NCBI36
NG_007729.1:g.51977G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703405.1:c.1081+1167G>C	ENSP00000515291.1:n.1081+1167G>C
ENST00000341462.9:c.1014G>C	ENSP00000340636.7:p.Thr338=
ENST00000425967.8:c.1014G>C	ENSP00000393312.4:p.Thr338=
ENST00000683765.1:c.1206G>C	ENSP00000507039.1:p.Thr402=
ENST00000683815.1:c.1014G>C	ENSP00000507997.1:p.Thr338=
ENST00000683948.1:n.1714G>C
ENST00000684654.1:c.747G>C	ENSP00000507205.1:p.Thr249=
ENST00000447712.7:c.1020G>C MANE Select	ENSP00000400162.2:p.Thr340=
ENST00000649678.1:c.1014G>C	ENSP00000497266.1:p.Thr338=
ENST00000674189.1:c.*672G>C	ENSP00000501345.1:n.*672G>C
ENST00000674217.1:n.1433G>C
ENST00000674235.1:c.807G>C
ENST00000674380.1:c.*987G>C	ENSP00000501514.1:n.*987G>C
ENST00000674474.1:n.2514G>C
ENST00000326324.10:c.747G>C	ENSP00000327229.6:p.Thr249=
ENST00000335922.9:c.996G>C	ENSP00000337247.5:p.Thr332=
ENST00000341462.8:c.*70G>C	ENSP00000340636.6:n.*70G>C
ENST00000356207.9:c.753G>C	ENSP00000348537.5:p.Thr251=
ENST00000397091.9:c.1014G>C	ENSP00000380280.5:p.Thr338=
ENST00000397103.5:c.814+1167G>C	ENSP00000380292.1:n.814+1167G>C
ENST00000397108.8:c.1014G>C	ENSP00000380297.4:p.Thr338=
ENST00000397113.6:c.1014G>C	ENSP00000380302.2:p.Thr338=
ENST00000425967.7:c.1113G>C	ENSP00000393312.3:p.Thr371=
ENST00000447712.6:c.1020G>C	ENSP00000400162.2:p.Thr340=
ENST00000466021.5:n.187G>C
ENST00000475621.1:n.335G>C
ENST00000487647.5:c.897G>C	ENSP00000435254.1:n.897G>C
ENST00000526570.5:n.3299G>C
ENST00000530701.1:n.261G>C
ENST00000532791.5:c.1020G>C	ENSP00000432972.1:p.Thr340=
ENST00000619564.3:c.664-2123G>C	ENSP00000484553.1:n.664-2123G>C
NM_001174063.1:c.1020G>C	NP_001167534.1:p.Thr340=
NM_001174064.1:c.996G>C	NP_001167535.1:p.Thr332=
NM_001174065.1:c.1014G>C	NP_001167536.1:p.Thr338=
NM_001174066.1:c.753G>C	NP_001167537.1:p.Thr251=
NM_001174067.1:c.1113G>C	NP_001167538.1:p.Thr371=
NM_015850.3:c.1014G>C	NP_056934.2:p.Thr338=
NM_023105.2:c.753G>C	NP_075593.1:p.Thr251=
NM_023106.2:c.747G>C	NP_075594.1:p.Thr249=
NM_023110.2:c.1020G>C	NP_075598.2:p.Thr340=
XM_006716303.2:c.1020G>C	XP_006716366.1:p.Thr340=
XM_006716304.1:c.1020G>C	XP_006716367.1:p.Thr340=
XM_006716305.2:c.1020G>C	XP_006716368.1:p.Thr340=
XM_006716306.2:c.1014G>C	XP_006716369.1:p.Thr338=
XM_006716307.1:c.1014G>C	XP_006716370.1:p.Thr338=
XM_006716309.2:c.996G>C	XP_006716372.1:p.Thr332=
XM_006716310.2:c.753G>C	XP_006716373.1:p.Thr251=
XM_006716311.1:c.753G>C	XP_006716374.1:p.Thr251=
XM_006716312.1:c.753G>C	XP_006716375.1:p.Thr251=
XM_006716313.2:c.747G>C	XP_006716376.1:p.Thr249=
XM_006716314.1:c.747G>C	XP_006716377.1:p.Thr249=
XM_011544443.1:c.1119G>C	XP_011542745.1:p.Thr373=
XM_011544444.1:c.1113G>C	XP_011542746.1:p.Thr371=
XM_011544445.1:c.1119G>C	XP_011542747.1:p.Thr373=
XM_011544446.1:c.1119G>C	XP_011542748.1:p.Thr373=
XM_011544447.1:c.1119G>C	XP_011542749.1:p.Thr373=
XM_011544448.1:c.852G>C	XP_011542750.1:p.Thr284=
XM_011544449.1:c.846G>C	XP_011542751.1:p.Thr282=
XM_011544450.1:c.846G>C	XP_011542752.1:p.Thr282=
XM_011544451.1:c.729G>C	XP_011542753.1:p.Thr243=
NM_001354367.1:c.1014G>C	NP_001341296.1:p.Thr338=
NM_001354368.1:c.747G>C	NP_001341297.1:p.Thr249=
NM_001354369.1:c.1014G>C	NP_001341298.1:p.Thr338=
NM_001354370.1:c.747G>C	NP_001341299.1:p.Thr249=
XM_006716303.3:c.1020G>C	XP_006716366.1:p.Thr340=
XM_006716310.3:c.753G>C	XP_006716373.1:p.Thr251=
XM_006716312.2:c.753G>C	XP_006716375.1:p.Thr251=
XM_006716314.2:c.747G>C	XP_006716377.1:p.Thr249=
XM_011544443.2:c.1119G>C	XP_011542745.1:p.Thr373=
XM_011544445.2:c.1119G>C	XP_011542747.1:p.Thr373=
XM_011544446.2:c.1119G>C	XP_011542748.1:p.Thr373=
XM_011544447.2:c.1119G>C	XP_011542749.1:p.Thr373=
XM_011544450.2:c.846G>C	XP_011542752.1:p.Thr282=
XM_017013219.1:c.1113G>C	XP_016868708.1:p.Thr371=
XM_017013220.1:c.1113G>C	XP_016868709.1:p.Thr371=
XM_017013221.1:c.1020G>C	XP_016868710.1:p.Thr340=
XM_017013222.2:c.1020G>C	XP_016868711.1:p.Thr340=
XM_017013224.2:c.1014G>C	XP_016868713.1:p.Thr338=
XM_017013225.2:c.1014G>C	XP_016868714.1:p.Thr338=
XM_017013226.1:c.852G>C	XP_016868715.1:p.Thr284=
XM_017013227.1:c.846G>C	XP_016868716.1:p.Thr282=
XM_017013229.2:c.54G>C	XP_016868718.1:p.Thr18=
XM_017013230.1:c.54G>C	XP_016868719.1:p.Thr18=
XM_024447097.1:c.996G>C	XP_024302865.1:p.Thr332=
XR_001745495.1:n.1268G>C
XR_001745496.1:n.1268G>C
NM_001174063.2:c.1020G>C	NP_001167534.1:p.Thr340=
NM_001174064.2:c.996G>C	NP_001167535.1:p.Thr332=
NM_001174065.2:c.1014G>C	NP_001167536.1:p.Thr338=
NM_001174066.2:c.753G>C	NP_001167537.1:p.Thr251=
NM_001354368.2:c.747G>C	NP_001341297.1:p.Thr249=
NM_015850.4:c.1014G>C	NP_056934.2:p.Thr338=
NM_023105.3:c.753G>C	NP_075593.1:p.Thr251=
NM_023106.3:c.747G>C	NP_075594.1:p.Thr249=
NM_023110.3:c.1020G>C MANE Select	NP_075598.2:p.Thr340=
NM_001174067.2:c.1113G>C	NP_001167538.1:p.Thr371=
NM_001354367.2:c.1014G>C	NP_001341296.1:p.Thr338=
NM_001354369.2:c.1014G>C	NP_001341298.1:p.Thr338=
NM_001354370.2:c.747G>C	NP_001341299.1:p.Thr249=