Canonical Allele Identifier: CA1603394659

Gene: FGFR4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177091149C= , CM000667.2:g.177091149C=	GRCh38
NC_000005.9:g.176518150C= , CM000667.1:g.176518150C=	GRCh37
NC_000005.8:g.176450756C=	NCBI36
NG_012067.1:g.9230C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.603+45C= MANE Select	ENSP00000292408.4:n.603+45C=
ENST00000292408.8:c.603+45C=	ENSP00000292408.4:n.603+45C=
ENST00000393637.5:c.603+45C=	ENSP00000377254.1:n.603+45C=
ENST00000393648.6:c.603+45C=	ENSP00000377259.2:n.603+45C=
ENST00000502906.5:c.603+45C=	ENSP00000424960.1:n.603+45C=
ENST00000509511.5:n.603+45C=
NM_001291980.1:c.603+45C=	NP_001278909.1:n.603+45C=
NM_002011.4:c.603+45C=	NP_002002.3:n.603+45C=
NM_022963.3:c.603+45C=	NP_075252.2:n.603+45C=
NM_213647.2:c.603+45C=	NP_998812.1:n.603+45C=
XM_005265838.2:c.603+45C=	XP_005265895.1:n.603+45C=
XM_011534464.1:c.696+45C=	XP_011532766.1:n.696+45C=
XM_011534465.1:c.285+45C=	XP_011532767.1:n.285+45C=
XR_941090.1:n.648+45C=
NM_001354984.1:c.603+45C=	NP_001341913.1:n.603+45C=
NM_213647.3:c.603+45C= MANE Select	NP_998812.1:n.603+45C=
NM_001291980.2:c.603+45C=	NP_001278909.1:n.603+45C=
NM_001354984.2:c.603+45C=	NP_001341913.1:n.603+45C=
NM_002011.5:c.603+45C=	NP_002002.3:n.603+45C=