Canonical Allele Identifier: CA1603396357

Gene: FGFR4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177092774G= , CM000667.2:g.177092774G=	GRCh38
NC_000005.9:g.176519775G= , CM000667.1:g.176519775G=	GRCh37
NC_000005.8:g.176452381G=	NCBI36
NG_012067.1:g.10855G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1047G= MANE Select	ENSP00000292408.4:p.Thr349=
ENST00000292408.8:c.1047G=	ENSP00000292408.4:p.Thr349=
ENST00000393637.5:c.1047G=	ENSP00000377254.1:p.Thr349=
ENST00000393648.6:c.1047G=	ENSP00000377259.2:p.Thr349=
ENST00000502906.5:c.1047G=	ENSP00000424960.1:p.Thr349=
ENST00000508139.1:n.351G=
ENST00000509511.5:n.1047G=
NM_001291980.1:c.1047G=	NP_001278909.1:p.Thr349=
NM_002011.4:c.1047G=	NP_002002.3:p.Thr349=
NM_022963.3:c.1047G=	NP_075252.2:p.Thr349=
NM_213647.2:c.1047G=	NP_998812.1:p.Thr349=
XM_005265838.2:c.1047G=	XP_005265895.1:p.Thr349=
XM_011534464.1:c.1140G=	XP_011532766.1:p.Thr380=
XM_011534465.1:c.729G=	XP_011532767.1:p.Thr243=
XR_941090.1:n.1092G=
NM_001354984.1:c.1047G=	NP_001341913.1:p.Thr349=
NM_213647.3:c.1047G= MANE Select	NP_998812.1:p.Thr349=
NM_001291980.2:c.1047G=	NP_001278909.1:p.Thr349=
NM_001354984.2:c.1047G=	NP_001341913.1:p.Thr349=
NM_002011.5:c.1047G=	NP_002002.3:p.Thr349=