Canonical Allele Identifier: CA1603407714
Gene: FGFR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177097539C= , CM000667.2:g.177097539C= GRCh38
NC_000005.9:g.176524540C= , CM000667.1:g.176524540C= GRCh37
NC_000005.8:g.176457146C= NCBI36
NG_012067.1:g.15620C=

Transcript Alleles

HGVS Amino-acid change
ENST00000292408.9:c.2272C= MANE Select ENSP00000292408.4:p.Arg758=
ENST00000292408.8:c.2272C= ENSP00000292408.4:p.Arg758=
ENST00000393637.5:c.2152C= ENSP00000377254.1:p.Arg718=
ENST00000393648.6:c.2068C= ENSP00000377259.2:p.Arg690=
ENST00000502906.5:c.2272C= ENSP00000424960.1:p.Arg758=
ENST00000513423.1:n.220C=
NM_001291980.1:c.2068C= NP_001278909.1:p.Arg690=
NM_002011.4:c.2272C= NP_002002.3:p.Arg758=
NM_022963.3:c.2152C= NP_075252.2:p.Arg718=
NM_213647.2:c.2272C= NP_998812.1:p.Arg758=
XM_005265838.2:c.2272C= XP_005265895.1:p.Arg758=
XM_011534464.1:c.2365C= XP_011532766.1:p.Arg789=
XM_011534465.1:c.1954C= XP_011532767.1:p.Arg652=
NM_001354984.1:c.2272C= NP_001341913.1:p.Arg758=
NM_213647.3:c.2272C= MANE Select NP_998812.1:p.Arg758=
NM_001291980.2:c.2068C= NP_001278909.1:p.Arg690=
NM_001354984.2:c.2272C= NP_001341913.1:p.Arg758=
NM_002011.5:c.2272C= NP_002002.3:p.Arg758=