Canonical Allele Identifier: CA564898723
Gene: FGFR4 HGNC NCBI

Linked Data

dbSNP Id: rs1457408963

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177093258_177093271del , CM000667.2:g.177093258_177093271del GRCh38
NC_000005.9:g.176520259_176520272del , CM000667.1:g.176520259_176520272del GRCh37
NC_000005.8:g.176452865_176452878del NCBI36
NG_012067.1:g.11339_11352del

Transcript Alleles

HGVS Amino-acid change
ENST00000292408.9:c.1178_1191del MANE Select ENSP00000292408.4:p.Gln393ProfsTer?
ENST00000292408.8:c.1178_1191del ENSP00000292408.4:p.Gln393ProfsTer?
ENST00000393637.5:c.1058-74_1058-61del ENSP00000377254.1:n.1058-74_1058-61del
ENST00000393648.6:c.1097+81_1097+94del ENSP00000377259.2:n.1097+81_1097+94del
ENST00000502906.5:c.1178_1191del ENSP00000424960.1:p.Gln393ProfsTer?
ENST00000508139.1:n.482_495del
ENST00000511076.1:c.84_97del
NM_001291980.1:c.1097+81_1097+94del NP_001278909.1:n.1097+81_1097+94del
NM_002011.4:c.1178_1191del NP_002002.3:p.Gln393ProfsTer?
NM_022963.3:c.1058-74_1058-61del NP_075252.2:n.1058-74_1058-61del
NM_213647.2:c.1178_1191del NP_998812.1:p.Gln393ProfsTer?
XM_005265838.2:c.1178_1191del XP_005265895.1:p.Gln393ProfsTer?
XM_011534464.1:c.1271_1284del XP_011532766.1:p.Gln424ProfsTer?
XM_011534465.1:c.860_873del XP_011532767.1:p.Gln287ProfsTer?
XR_941090.1:n.1223_1236del
NM_001354984.1:c.1178_1191del NP_001341913.1:p.Gln393ProfsTer?
NM_213647.3:c.1178_1191del MANE Select NP_998812.1:p.Gln393ProfsTer?
NM_001291980.2:c.1097+81_1097+94del NP_001278909.1:n.1097+81_1097+94del
NM_001354984.2:c.1178_1191del NP_001341913.1:p.Gln393ProfsTer?
NM_002011.5:c.1178_1191del NP_002002.3:p.Gln393ProfsTer?