Canonical Allele Identifier: CA447959206

Gene: FGFR4

Linked Data

• dbSNP Id: rs2149731144
• MyVariant Identifiers: chr5:g.176517653T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177090652T>C , CM000667.2:g.177090652T>C	GRCh38
NC_000005.9:g.176517653T>C , CM000667.1:g.176517653T>C	GRCh37
NC_000005.8:g.176450259T>C	NCBI36
NG_012067.1:g.8733T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.354T>C MANE Select	ENSP00000292408.4:p.Gly118=
ENST00000292408.8:c.354T>C	ENSP00000292408.4:p.Gly118=
ENST00000393637.5:c.354T>C	ENSP00000377254.1:p.Gly118=
ENST00000393648.6:c.354T>C	ENSP00000377259.2:p.Gly118=
ENST00000426612.5:n.359T>C
ENST00000430285.5:c.*218T>C	ENSP00000395164.1:n.*218T>C
ENST00000502906.5:c.354T>C	ENSP00000424960.1:p.Gly118=
ENST00000503708.5:c.354T>C	ENSP00000424905.1:p.Gly118=
ENST00000509511.5:n.354T>C
NM_001291980.1:c.354T>C	NP_001278909.1:p.Gly118=
NM_002011.4:c.354T>C	NP_002002.3:p.Gly118=
NM_022963.3:c.354T>C	NP_075252.2:p.Gly118=
NM_213647.2:c.354T>C	NP_998812.1:p.Gly118=
XM_005265838.2:c.354T>C	XP_005265895.1:p.Gly118=
XM_011534464.1:c.447T>C	XP_011532766.1:p.Gly149=
XM_011534465.1:c.36T>C	XP_011532767.1:p.Gly12=
XR_941090.1:n.399T>C
NM_001354984.1:c.354T>C	NP_001341913.1:p.Gly118=
NM_213647.3:c.354T>C MANE Select	NP_998812.1:p.Gly118=
NM_001291980.2:c.354T>C	NP_001278909.1:p.Gly118=
NM_001354984.2:c.354T>C	NP_001341913.1:p.Gly118=
NM_002011.5:c.354T>C	NP_002002.3:p.Gly118=