Canonical Allele Identifier: CA1603397363

Gene: FGFR4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093485C= , CM000667.2:g.177093485C=	GRCh38
NC_000005.9:g.176520486C= , CM000667.1:g.176520486C=	GRCh37
NC_000005.8:g.176453092C=	NCBI36
NG_012067.1:g.11566C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1331C= MANE Select	ENSP00000292408.4:p.Ala444=
ENST00000292408.8:c.1331C=	ENSP00000292408.4:p.Ala444=
ENST00000393637.5:c.1211C=	ENSP00000377254.1:p.Ala404=
ENST00000393648.6:c.1177C=	ENSP00000377259.2:p.Pro393=
ENST00000502906.5:c.1331C=	ENSP00000424960.1:p.Ala444=
ENST00000508139.1:n.709C=
ENST00000511076.1:c.225C=
NM_001291980.1:c.1177C=	NP_001278909.1:p.Pro393=
NM_002011.4:c.1331C=	NP_002002.3:p.Ala444=
NM_022963.3:c.1211C=	NP_075252.2:p.Ala404=
NM_213647.2:c.1331C=	NP_998812.1:p.Ala444=
XM_005265838.2:c.1331C=	XP_005265895.1:p.Ala444=
XM_011534464.1:c.1424C=	XP_011532766.1:p.Ala475=
XM_011534465.1:c.1013C=	XP_011532767.1:p.Ala338=
XR_941090.1:n.1376C=
NM_001354984.1:c.1331C=	NP_001341913.1:p.Ala444=
NM_213647.3:c.1331C= MANE Select	NP_998812.1:p.Ala444=
NM_001291980.2:c.1177C=	NP_001278909.1:p.Pro393=
NM_001354984.2:c.1331C=	NP_001341913.1:p.Ala444=
NM_002011.5:c.1331C=	NP_002002.3:p.Ala444=