Canonical Allele Identifier: CA1603397184

Gene: FGFR4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093352C= , CM000667.2:g.177093352C=	GRCh38
NC_000005.9:g.176520353C= , CM000667.1:g.176520353C=	GRCh37
NC_000005.8:g.176452959C=	NCBI36
NG_012067.1:g.11433C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1251+21C= MANE Select	ENSP00000292408.4:n.1251+21C=
ENST00000292408.8:c.1251+21C=	ENSP00000292408.4:n.1251+21C=
ENST00000393637.5:c.1078C=	ENSP00000377254.1:p.Leu360=
ENST00000393648.6:c.1098-54C=	ENSP00000377259.2:n.1098-54C=
ENST00000502906.5:c.1251+21C=	ENSP00000424960.1:n.1251+21C=
ENST00000508139.1:n.576C=
ENST00000511076.1:c.157+21C=
NM_001291980.1:c.1098-54C=	NP_001278909.1:n.1098-54C=
NM_002011.4:c.1251+21C=	NP_002002.3:n.1251+21C=
NM_022963.3:c.1078C=	NP_075252.2:p.Leu360=
NM_213647.2:c.1251+21C=	NP_998812.1:n.1251+21C=
XM_005265838.2:c.1251+21C=	XP_005265895.1:n.1251+21C=
XM_011534464.1:c.1344+21C=	XP_011532766.1:n.1344+21C=
XM_011534465.1:c.933+21C=	XP_011532767.1:n.933+21C=
XR_941090.1:n.1296+21C=
NM_001354984.1:c.1251+21C=	NP_001341913.1:n.1251+21C=
NM_213647.3:c.1251+21C= MANE Select	NP_998812.1:n.1251+21C=
NM_001291980.2:c.1098-54C=	NP_001278909.1:n.1098-54C=
NM_001354984.2:c.1251+21C=	NP_001341913.1:n.1251+21C=
NM_002011.5:c.1251+21C=	NP_002002.3:n.1251+21C=