Canonical Allele Identifier: CA1603397349

Gene: FGFR4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093478G= , CM000667.2:g.177093478G=	GRCh38
NC_000005.9:g.176520479G= , CM000667.1:g.176520479G=	GRCh37
NC_000005.8:g.176453085G=	NCBI36
NG_012067.1:g.11559G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1324G= MANE Select	ENSP00000292408.4:p.Gly442=
ENST00000292408.8:c.1324G=	ENSP00000292408.4:p.Gly442=
ENST00000393637.5:c.1204G=	ENSP00000377254.1:p.Gly402=
ENST00000393648.6:c.1170G=	ENSP00000377259.2:p.Ala390=
ENST00000502906.5:c.1324G=	ENSP00000424960.1:p.Gly442=
ENST00000508139.1:n.702G=
ENST00000511076.1:c.218G=
NM_001291980.1:c.1170G=	NP_001278909.1:p.Ala390=
NM_002011.4:c.1324G=	NP_002002.3:p.Gly442=
NM_022963.3:c.1204G=	NP_075252.2:p.Gly402=
NM_213647.2:c.1324G=	NP_998812.1:p.Gly442=
XM_005265838.2:c.1324G=	XP_005265895.1:p.Gly442=
XM_011534464.1:c.1417G=	XP_011532766.1:p.Gly473=
XM_011534465.1:c.1006G=	XP_011532767.1:p.Gly336=
XR_941090.1:n.1369G=
NM_001354984.1:c.1324G=	NP_001341913.1:p.Gly442=
NM_213647.3:c.1324G= MANE Select	NP_998812.1:p.Gly442=
NM_001291980.2:c.1170G=	NP_001278909.1:p.Ala390=
NM_001354984.2:c.1324G=	NP_001341913.1:p.Gly442=
NM_002011.5:c.1324G=	NP_002002.3:p.Gly442=