Canonical Allele Identifier: CA2711100918

Gene: FGFR4

Linked Data

• dbSNP Id: rs2149735443

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093291_177093292insG , CM000667.2:g.177093291_177093292insG	GRCh38
NC_000005.9:g.176520292_176520293insG , CM000667.1:g.176520292_176520293insG	GRCh37
NC_000005.8:g.176452898_176452899insG	NCBI36
NG_012067.1:g.11372_11373insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1211_1212insG MANE Select	ENSP00000292408.4:p.Thr405HisfsTer?
ENST00000292408.8:c.1211_1212insG	ENSP00000292408.4:p.Thr405HisfsTer?
ENST00000393637.5:c.1058-41_1058-40insG	ENSP00000377254.1:n.1058-41_1058-40insG
ENST00000393648.6:c.1098-115_1098-114insG	ENSP00000377259.2:n.1098-115_1098-114insG
ENST00000502906.5:c.1211_1212insG	ENSP00000424960.1:p.Thr405HisfsTer?
ENST00000508139.1:n.515_516insG
ENST00000511076.1:c.117_118insG
NM_001291980.1:c.1098-115_1098-114insG	NP_001278909.1:n.1098-115_1098-114insG
NM_002011.4:c.1211_1212insG	NP_002002.3:p.Thr405HisfsTer?
NM_022963.3:c.1058-41_1058-40insG	NP_075252.2:n.1058-41_1058-40insG
NM_213647.2:c.1211_1212insG	NP_998812.1:p.Thr405HisfsTer?
XM_005265838.2:c.1211_1212insG	XP_005265895.1:p.Thr405HisfsTer?
XM_011534464.1:c.1304_1305insG	XP_011532766.1:p.Thr436HisfsTer?
XM_011534465.1:c.893_894insG	XP_011532767.1:p.Thr299HisfsTer?
XR_941090.1:n.1256_1257insG
NM_001354984.1:c.1211_1212insG	NP_001341913.1:p.Thr405HisfsTer?
NM_213647.3:c.1211_1212insG MANE Select	NP_998812.1:p.Thr405HisfsTer?
NM_001291980.2:c.1098-115_1098-114insG	NP_001278909.1:n.1098-115_1098-114insG
NM_001354984.2:c.1211_1212insG	NP_001341913.1:p.Thr405HisfsTer?
NM_002011.5:c.1211_1212insG	NP_002002.3:p.Thr405HisfsTer?