Canonical Allele Identifier: CA1603394470

Gene: FGFR4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177090990T= , CM000667.2:g.177090990T=	GRCh38
NC_000005.9:g.176517991T= , CM000667.1:g.176517991T=	GRCh37
NC_000005.8:g.176450597T=	NCBI36
NG_012067.1:g.9071T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.489T= MANE Select	ENSP00000292408.4:p.Pro163=
ENST00000292408.8:c.489T=	ENSP00000292408.4:p.Pro163=
ENST00000393637.5:c.489T=	ENSP00000377254.1:p.Pro163=
ENST00000393648.6:c.489T=	ENSP00000377259.2:p.Pro163=
ENST00000426612.5:n.606T=
ENST00000430285.5:c.*353T=	ENSP00000395164.1:n.*353T=
ENST00000502906.5:c.489T=	ENSP00000424960.1:p.Pro163=
ENST00000503708.5:c.489T=	ENSP00000424905.1:p.Pro163=
ENST00000509511.5:n.489T=
NM_001291980.1:c.489T=	NP_001278909.1:p.Pro163=
NM_002011.4:c.489T=	NP_002002.3:p.Pro163=
NM_022963.3:c.489T=	NP_075252.2:p.Pro163=
NM_213647.2:c.489T=	NP_998812.1:p.Pro163=
XM_005265838.2:c.489T=	XP_005265895.1:p.Pro163=
XM_011534464.1:c.582T=	XP_011532766.1:p.Pro194=
XM_011534465.1:c.171T=	XP_011532767.1:p.Pro57=
XR_941090.1:n.534T=
NM_001354984.1:c.489T=	NP_001341913.1:p.Pro163=
NM_213647.3:c.489T= MANE Select	NP_998812.1:p.Pro163=
NM_001291980.2:c.489T=	NP_001278909.1:p.Pro163=
NM_001354984.2:c.489T=	NP_001341913.1:p.Pro163=
NM_002011.5:c.489T=	NP_002002.3:p.Pro163=