Canonical Allele Identifier: CA1603397480

Gene: FGFR4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093551G= , CM000667.2:g.177093551G=	GRCh38
NC_000005.9:g.176520552G= , CM000667.1:g.176520552G=	GRCh37
NC_000005.8:g.176453158G=	NCBI36
NG_012067.1:g.11632G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1397G= MANE Select	ENSP00000292408.4:p.Arg466=
ENST00000292408.8:c.1397G=	ENSP00000292408.4:p.Arg466=
ENST00000393637.5:c.1277G=	ENSP00000377254.1:p.Arg426=
ENST00000393648.6:c.1193+50G=	ENSP00000377259.2:n.1193+50G=
ENST00000502906.5:c.1397G=	ENSP00000424960.1:p.Arg466=
ENST00000511076.1:c.291G=
NM_001291980.1:c.1193+50G=	NP_001278909.1:n.1193+50G=
NM_002011.4:c.1397G=	NP_002002.3:p.Arg466=
NM_022963.3:c.1277G=	NP_075252.2:p.Arg426=
NM_213647.2:c.1397G=	NP_998812.1:p.Arg466=
XM_005265838.2:c.1397G=	XP_005265895.1:p.Arg466=
XM_011534464.1:c.1490G=	XP_011532766.1:p.Arg497=
XM_011534465.1:c.1079G=	XP_011532767.1:p.Arg360=
XR_941090.1:n.1392+50G=
NM_001354984.1:c.1397G=	NP_001341913.1:p.Arg466=
NM_213647.3:c.1397G= MANE Select	NP_998812.1:p.Arg466=
NM_001291980.2:c.1193+50G=	NP_001278909.1:n.1193+50G=
NM_001354984.2:c.1397G=	NP_001341913.1:p.Arg466=
NM_002011.5:c.1397G=	NP_002002.3:p.Arg466=