Canonical Allele Identifier: CA1603396773
Gene: FGFR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177093150C= , CM000667.2:g.177093150C= GRCh38
NC_000005.9:g.176520151C= , CM000667.1:g.176520151C= GRCh37
NC_000005.8:g.176452757C= NCBI36
NG_012067.1:g.11231C=

Transcript Alleles

HGVS Amino-acid change
ENST00000292408.9:c.1070C= MANE Select ENSP00000292408.4:p.Thr357=
ENST00000292408.8:c.1070C= ENSP00000292408.4:p.Thr357=
ENST00000393637.5:c.1058-182C= ENSP00000377254.1:n.1058-182C=
ENST00000393648.6:c.1070C= ENSP00000377259.2:p.Thr357=
ENST00000502906.5:c.1070C= ENSP00000424960.1:p.Thr357=
ENST00000508139.1:n.374C=
NM_001291980.1:c.1070C= NP_001278909.1:p.Thr357=
NM_002011.4:c.1070C= NP_002002.3:p.Thr357=
NM_022963.3:c.1058-182C= NP_075252.2:n.1058-182C=
NM_213647.2:c.1070C= NP_998812.1:p.Thr357=
XM_005265838.2:c.1070C= XP_005265895.1:p.Thr357=
XM_011534464.1:c.1163C= XP_011532766.1:p.Thr388=
XM_011534465.1:c.752C= XP_011532767.1:p.Thr251=
XR_941090.1:n.1115C=
NM_001354984.1:c.1070C= NP_001341913.1:p.Thr357=
NM_213647.3:c.1070C= MANE Select NP_998812.1:p.Thr357=
NM_001291980.2:c.1070C= NP_001278909.1:p.Thr357=
NM_001354984.2:c.1070C= NP_001341913.1:p.Thr357=
NM_002011.5:c.1070C= NP_002002.3:p.Thr357=