Canonical Allele Identifier: CA1603404231

Gene: FGFR4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177095415C= , CM000667.2:g.177095415C=	GRCh38
NC_000005.9:g.176522416C= , CM000667.1:g.176522416C=	GRCh37
NC_000005.8:g.176455022C=	NCBI36
NG_012067.1:g.13496C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1605C= MANE Select	ENSP00000292408.4:p.Asn535=
ENST00000292408.8:c.1605C=	ENSP00000292408.4:p.Asn535=
ENST00000393637.5:c.1485C=	ENSP00000377254.1:p.Asn495=
ENST00000393648.6:c.1401C=	ENSP00000377259.2:p.Asn467=
ENST00000483872.2:n.591C=
ENST00000502906.5:c.1605C=	ENSP00000424960.1:p.Asn535=
ENST00000511076.1:c.499C=
NM_001291980.1:c.1401C=	NP_001278909.1:p.Asn467=
NM_002011.4:c.1605C=	NP_002002.3:p.Asn535=
NM_022963.3:c.1485C=	NP_075252.2:p.Asn495=
NM_213647.2:c.1605C=	NP_998812.1:p.Asn535=
XM_005265838.2:c.1605C=	XP_005265895.1:p.Asn535=
XM_011534464.1:c.1698C=	XP_011532766.1:p.Asn566=
XM_011534465.1:c.1287C=	XP_011532767.1:p.Asn429=
XR_941090.1:n.1600C=
NM_001354984.1:c.1605C=	NP_001341913.1:p.Asn535=
NM_213647.3:c.1605C= MANE Select	NP_998812.1:p.Asn535=
NM_001291980.2:c.1401C=	NP_001278909.1:p.Asn467=
NM_001354984.2:c.1605C=	NP_001341913.1:p.Asn535=
NM_002011.5:c.1605C=	NP_002002.3:p.Asn535=