Canonical Allele Identifier: CA1603392888

Gene: FGFR4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177089630G= , CM000667.2:g.177089630G=	GRCh38
NC_000005.9:g.176516631G= , CM000667.1:g.176516631G=	GRCh37
NC_000005.8:g.176449237G=	NCBI36
NG_012067.1:g.7711G=

Transcript Alleles

HGVS	Amino-acid Change
NM_213647.3:c.28G= MANE Select	NP_998812.1:p.Val10=
ENST00000292408.9:c.28G= MANE Select	ENSP00000292408.4:p.Val10=
NM_001291980.1:c.28G=	NP_001278909.1:p.Val10=
NM_001291980.2:c.28G=	NP_001278909.1:p.Val10=
NM_001354984.1:c.28G=	NP_001341913.1:p.Val10=
NM_001354984.2:c.28G=	NP_001341913.1:p.Val10=
NM_002011.4:c.28G=	NP_002002.3:p.Val10=
NM_002011.5:c.28G=	NP_002002.3:p.Val10=
NM_022963.3:c.28G=	NP_075252.2:p.Val10=
NM_213647.2:c.28G=	NP_998812.1:p.Val10=
ENST00000292408.8:c.28G=	ENSP00000292408.4:p.Val10=
ENST00000393637.5:c.28G=	ENSP00000377254.1:p.Val10=
ENST00000393648.6:c.28G=	ENSP00000377259.2:p.Val10=
ENST00000426612.5:n.33G=
ENST00000430285.5:c.28G=	ENSP00000395164.1:p.Val10=
ENST00000502906.5:c.28G=	ENSP00000424960.1:p.Val10=
ENST00000503708.5:c.28G=	ENSP00000424905.1:p.Val10=
ENST00000507708.1:n.184G=
ENST00000509511.5:n.28G=
ENST00000510911.5:c.28G=	ENSP00000427222.1:p.Val10=
ENST00000513166.1:c.28G=	ENSP00000422889.1:p.Val10=
ENST00000514472.1:c.28G=	ENSP00000426492.1:p.Val10=
XM_005265838.2:c.28G=	XP_005265895.1:p.Val10=
XM_011534464.1:c.121G=	XP_011532766.1:p.Val41=
XM_011534465.1:c.-346G=	XP_011532767.1:n.-346G=
XR_941090.1:n.73G=