Canonical Allele Identifier: CA3576275
Gene: FGFR4 HGNC NCBI

Linked Data

dbSNP Id: rs375477942

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177093192T>G , CM000667.2:g.177093192T>G GRCh38
NC_000005.9:g.176520193T>G , CM000667.1:g.176520193T>G GRCh37
NC_000005.8:g.176452799T>G NCBI36
NG_012067.1:g.11273T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000292408.9:c.1112T>G MANE Select ENSP00000292408.4:p.Ile371Ser
ENST00000292408.8:c.1112T>G ENSP00000292408.4:p.Ile371Ser
ENST00000393637.5:c.1058-140T>G ENSP00000377254.1:n.1058-140T>G
ENST00000393648.6:c.1097+15T>G ENSP00000377259.2:n.1097+15T>G
ENST00000502906.5:c.1112T>G ENSP00000424960.1:p.Ile371Ser
ENST00000508139.1:n.416T>G
ENST00000511076.1:c.18T>G
NM_001291980.1:c.1097+15T>G NP_001278909.1:n.1097+15T>G
NM_002011.4:c.1112T>G NP_002002.3:p.Ile371Ser
NM_022963.3:c.1058-140T>G NP_075252.2:n.1058-140T>G
NM_213647.2:c.1112T>G NP_998812.1:p.Ile371Ser
XM_005265838.2:c.1112T>G XP_005265895.1:p.Ile371Ser
XM_011534464.1:c.1205T>G XP_011532766.1:p.Ile402Ser
XM_011534465.1:c.794T>G XP_011532767.1:p.Ile265Ser
XR_941090.1:n.1157T>G
NM_001354984.1:c.1112T>G NP_001341913.1:p.Ile371Ser
NM_213647.3:c.1112T>G MANE Select NP_998812.1:p.Ile371Ser
NM_001291980.2:c.1097+15T>G NP_001278909.1:n.1097+15T>G
NM_001354984.2:c.1112T>G NP_001341913.1:p.Ile371Ser
NM_002011.5:c.1112T>G NP_002002.3:p.Ile371Ser