Canonical Allele Identifier: CA1603394547

Gene: FGFR4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177091047C= , CM000667.2:g.177091047C=	GRCh38
NC_000005.9:g.176518048C= , CM000667.1:g.176518048C=	GRCh37
NC_000005.8:g.176450654C=	NCBI36
NG_012067.1:g.9128C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.546C= MANE Select	ENSP00000292408.4:p.Ile182=
ENST00000292408.8:c.546C=	ENSP00000292408.4:p.Ile182=
ENST00000393637.5:c.546C=	ENSP00000377254.1:p.Ile182=
ENST00000393648.6:c.546C=	ENSP00000377259.2:p.Ile182=
ENST00000426612.5:n.663C=
ENST00000430285.5:c.*410C=	ENSP00000395164.1:n.*410C=
ENST00000502906.5:c.546C=	ENSP00000424960.1:p.Ile182=
ENST00000503708.5:c.546C=	ENSP00000424905.1:p.Ile182=
ENST00000509511.5:n.546C=
NM_001291980.1:c.546C=	NP_001278909.1:p.Ile182=
NM_002011.4:c.546C=	NP_002002.3:p.Ile182=
NM_022963.3:c.546C=	NP_075252.2:p.Ile182=
NM_213647.2:c.546C=	NP_998812.1:p.Ile182=
XM_005265838.2:c.546C=	XP_005265895.1:p.Ile182=
XM_011534464.1:c.639C=	XP_011532766.1:p.Ile213=
XM_011534465.1:c.228C=	XP_011532767.1:p.Ile76=
XR_941090.1:n.591C=
NM_001354984.1:c.546C=	NP_001341913.1:p.Ile182=
NM_213647.3:c.546C= MANE Select	NP_998812.1:p.Ile182=
NM_001291980.2:c.546C=	NP_001278909.1:p.Ile182=
NM_001354984.2:c.546C=	NP_001341913.1:p.Ile182=
NM_002011.5:c.546C=	NP_002002.3:p.Ile182=