Canonical Allele Identifier: CA1603407766

Gene: FGFR4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177097556C= , CM000667.2:g.177097556C=	GRCh38
NC_000005.9:g.176524557C= , CM000667.1:g.176524557C=	GRCh37
NC_000005.8:g.176457163C=	NCBI36
NG_012067.1:g.15637C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.2289C= MANE Select	ENSP00000292408.4:p.Pro763=
ENST00000292408.8:c.2289C=	ENSP00000292408.4:p.Pro763=
ENST00000393637.5:c.2169C=	ENSP00000377254.1:p.Pro723=
ENST00000393648.6:c.2085C=	ENSP00000377259.2:p.Pro695=
ENST00000502906.5:c.2289C=	ENSP00000424960.1:p.Pro763=
ENST00000513423.1:n.237C=
NM_001291980.1:c.2085C=	NP_001278909.1:p.Pro695=
NM_002011.4:c.2289C=	NP_002002.3:p.Pro763=
NM_022963.3:c.2169C=	NP_075252.2:p.Pro723=
NM_213647.2:c.2289C=	NP_998812.1:p.Pro763=
XM_005265838.2:c.2289C=	XP_005265895.1:p.Pro763=
XM_011534464.1:c.2382C=	XP_011532766.1:p.Pro794=
XM_011534465.1:c.1971C=	XP_011532767.1:p.Pro657=
NM_001354984.1:c.2289C=	NP_001341913.1:p.Pro763=
NM_213647.3:c.2289C= MANE Select	NP_998812.1:p.Pro763=
NM_001291980.2:c.2085C=	NP_001278909.1:p.Pro695=
NM_001354984.2:c.2289C=	NP_001341913.1:p.Pro763=
NM_002011.5:c.2289C=	NP_002002.3:p.Pro763=