Canonical Allele Identifier: CA1603404306

Gene: FGFR4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177095559G= , CM000667.2:g.177095559G=	GRCh38
NC_000005.9:g.176522560G= , CM000667.1:g.176522560G=	GRCh37
NC_000005.8:g.176455166G=	NCBI36
NG_012067.1:g.13640G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000292408.9:c.1657G= MANE Select	ENSP00000292408.4:p.Ala553=
ENST00000292408.8:c.1657G=	ENSP00000292408.4:p.Ala553=
ENST00000393637.5:c.1537G=	ENSP00000377254.1:p.Ala513=
ENST00000393648.6:c.1453G=	ENSP00000377259.2:p.Ala485=
ENST00000483872.2:n.643G=
ENST00000502906.5:c.1657G=	ENSP00000424960.1:p.Ala553=
ENST00000511076.1:c.551G=
NM_001291980.1:c.1453G=	NP_001278909.1:p.Ala485=
NM_002011.4:c.1657G=	NP_002002.3:p.Ala553=
NM_022963.3:c.1537G=	NP_075252.2:p.Ala513=
NM_213647.2:c.1657G=	NP_998812.1:p.Ala553=
XM_005265838.2:c.1657G=	XP_005265895.1:p.Ala553=
XM_011534464.1:c.1750G=	XP_011532766.1:p.Ala584=
XM_011534465.1:c.1339G=	XP_011532767.1:p.Ala447=
XR_941090.1:n.1652G=
NM_001354984.1:c.1657G=	NP_001341913.1:p.Ala553=
NM_213647.3:c.1657G= MANE Select	NP_998812.1:p.Ala553=
NM_001291980.2:c.1453G=	NP_001278909.1:p.Ala485=
NM_001354984.2:c.1657G=	NP_001341913.1:p.Ala553=
NM_002011.5:c.1657G=	NP_002002.3:p.Ala553=