Canonical Allele Identifier: CA362299841

Gene: FGFR4

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177097601C>A , CM000667.2:g.177097601C>A	GRCh38
NC_000005.9:g.176524602C>A , CM000667.1:g.176524602C>A	GRCh37
NC_000005.8:g.176457208C>A	NCBI36
NG_012067.1:g.15682C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.2334C>A MANE Select	ENSP00000292408.4:p.Ser778Arg
ENST00000292408.8:c.2334C>A	ENSP00000292408.4:p.Ser778Arg
ENST00000393637.5:c.2214C>A	ENSP00000377254.1:p.Ser738Arg
ENST00000393648.6:c.2130C>A	ENSP00000377259.2:p.Ser710Arg
ENST00000502906.5:c.2334C>A	ENSP00000424960.1:p.Ser778Arg
ENST00000513423.1:n.282C>A
NM_001291980.1:c.2130C>A	NP_001278909.1:p.Ser710Arg
NM_002011.4:c.2334C>A	NP_002002.3:p.Ser778Arg
NM_022963.3:c.2214C>A	NP_075252.2:p.Ser738Arg
NM_213647.2:c.2334C>A	NP_998812.1:p.Ser778Arg
XM_005265838.2:c.2334C>A	XP_005265895.1:p.Ser778Arg
XM_011534464.1:c.2427C>A	XP_011532766.1:p.Ser809Arg
XM_011534465.1:c.2016C>A	XP_011532767.1:p.Ser672Arg
NM_001354984.1:c.2334C>A	NP_001341913.1:p.Ser778Arg
NM_213647.3:c.2334C>A MANE Select	NP_998812.1:p.Ser778Arg
NM_001291980.2:c.2130C>A	NP_001278909.1:p.Ser710Arg
NM_001354984.2:c.2334C>A	NP_001341913.1:p.Ser778Arg
NM_002011.5:c.2334C>A	NP_002002.3:p.Ser778Arg