Canonical Allele Identifier: CA447958758
Gene: FGFR4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.176520158C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177093157C>G , CM000667.2:g.177093157C>G GRCh38
NC_000005.9:g.176520158C>G , CM000667.1:g.176520158C>G GRCh37
NC_000005.8:g.176452764C>G NCBI36
NG_012067.1:g.11238C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000292408.9:c.1077C>G MANE Select ENSP00000292408.4:p.Thr359=
ENST00000292408.8:c.1077C>G ENSP00000292408.4:p.Thr359=
ENST00000393637.5:c.1058-175C>G ENSP00000377254.1:n.1058-175C>G
ENST00000393648.6:c.1077C>G ENSP00000377259.2:p.Thr359=
ENST00000502906.5:c.1077C>G ENSP00000424960.1:p.Thr359=
ENST00000508139.1:n.381C>G
NM_001291980.1:c.1077C>G NP_001278909.1:p.Thr359=
NM_002011.4:c.1077C>G NP_002002.3:p.Thr359=
NM_022963.3:c.1058-175C>G NP_075252.2:n.1058-175C>G
NM_213647.2:c.1077C>G NP_998812.1:p.Thr359=
XM_005265838.2:c.1077C>G XP_005265895.1:p.Thr359=
XM_011534464.1:c.1170C>G XP_011532766.1:p.Thr390=
XM_011534465.1:c.759C>G XP_011532767.1:p.Thr253=
XR_941090.1:n.1122C>G
NM_001354984.1:c.1077C>G NP_001341913.1:p.Thr359=
NM_213647.3:c.1077C>G MANE Select NP_998812.1:p.Thr359=
NM_001291980.2:c.1077C>G NP_001278909.1:p.Thr359=
NM_001354984.2:c.1077C>G NP_001341913.1:p.Thr359=
NM_002011.5:c.1077C>G NP_002002.3:p.Thr359=