Canonical Allele Identifier: CA1603407195

Gene: FGFR4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177097353C= , CM000667.2:g.177097353C=	GRCh38
NC_000005.9:g.176524354C= , CM000667.1:g.176524354C=	GRCh37
NC_000005.8:g.176456960C=	NCBI36
NG_012067.1:g.15434C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000292408.9:c.2215C= MANE Select	ENSP00000292408.4:p.Leu739=
ENST00000292408.8:c.2215C=	ENSP00000292408.4:p.Leu739=
ENST00000393637.5:c.2095C=	ENSP00000377254.1:p.Leu699=
ENST00000393648.6:c.2011C=	ENSP00000377259.2:p.Leu671=
ENST00000502906.5:c.2215C=	ENSP00000424960.1:p.Leu739=
ENST00000513423.1:n.163C=
NM_001291980.1:c.2011C=	NP_001278909.1:p.Leu671=
NM_002011.4:c.2215C=	NP_002002.3:p.Leu739=
NM_022963.3:c.2095C=	NP_075252.2:p.Leu699=
NM_213647.2:c.2215C=	NP_998812.1:p.Leu739=
XM_005265838.2:c.2215C=	XP_005265895.1:p.Leu739=
XM_011534464.1:c.2308C=	XP_011532766.1:p.Leu770=
XM_011534465.1:c.1897C=	XP_011532767.1:p.Leu633=
NM_001354984.1:c.2215C=	NP_001341913.1:p.Leu739=
NM_213647.3:c.2215C= MANE Select	NP_998812.1:p.Leu739=
NM_001291980.2:c.2011C=	NP_001278909.1:p.Leu671=
NM_001354984.2:c.2215C=	NP_001341913.1:p.Leu739=
NM_002011.5:c.2215C=	NP_002002.3:p.Leu739=