Canonical Allele Identifier: CA1603396781
Gene: FGFR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177093154G= , CM000667.2:g.177093154G= GRCh38
NC_000005.9:g.176520155G= , CM000667.1:g.176520155G= GRCh37
NC_000005.8:g.176452761G= NCBI36
NG_012067.1:g.11235G=

Transcript Alleles

HGVS Amino-acid change
ENST00000292408.9:c.1074G= MANE Select ENSP00000292408.4:p.Trp358=
ENST00000292408.8:c.1074G= ENSP00000292408.4:p.Trp358=
ENST00000393637.5:c.1058-178G= ENSP00000377254.1:n.1058-178G=
ENST00000393648.6:c.1074G= ENSP00000377259.2:p.Trp358=
ENST00000502906.5:c.1074G= ENSP00000424960.1:p.Trp358=
ENST00000508139.1:n.378G=
NM_001291980.1:c.1074G= NP_001278909.1:p.Trp358=
NM_002011.4:c.1074G= NP_002002.3:p.Trp358=
NM_022963.3:c.1058-178G= NP_075252.2:n.1058-178G=
NM_213647.2:c.1074G= NP_998812.1:p.Trp358=
XM_005265838.2:c.1074G= XP_005265895.1:p.Trp358=
XM_011534464.1:c.1167G= XP_011532766.1:p.Trp389=
XM_011534465.1:c.756G= XP_011532767.1:p.Trp252=
XR_941090.1:n.1119G=
NM_001354984.1:c.1074G= NP_001341913.1:p.Trp358=
NM_213647.3:c.1074G= MANE Select NP_998812.1:p.Trp358=
NM_001291980.2:c.1074G= NP_001278909.1:p.Trp358=
NM_001354984.2:c.1074G= NP_001341913.1:p.Trp358=
NM_002011.5:c.1074G= NP_002002.3:p.Trp358=