Canonical Allele Identifier: CA2676682073
Gene: FGFR4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177093281del , CM000667.2:g.177093281del GRCh38
NC_000005.9:g.176520282del , CM000667.1:g.176520282del GRCh37
NC_000005.8:g.176452888del NCBI36
NG_012067.1:g.11362del

Transcript Alleles

HGVS Amino-acid Change
ENST00000292408.9:c.1201del MANE Select ENSP00000292408.4:p.Arg401AlafsTer?
ENST00000292408.8:c.1201del ENSP00000292408.4:p.Arg401AlafsTer?
ENST00000393637.5:c.1058-51del ENSP00000377254.1:n.1058-51del
ENST00000393648.6:c.1097+104del ENSP00000377259.2:n.1097+104del
ENST00000502906.5:c.1201del ENSP00000424960.1:p.Arg401AlafsTer?
ENST00000508139.1:n.505del
ENST00000511076.1:c.107del
NM_001291980.1:c.1097+104del NP_001278909.1:n.1097+104del
NM_002011.4:c.1201del NP_002002.3:p.Arg401AlafsTer?
NM_022963.3:c.1058-51del NP_075252.2:n.1058-51del
NM_213647.2:c.1201del NP_998812.1:p.Arg401AlafsTer?
XM_005265838.2:c.1201del XP_005265895.1:p.Arg401AlafsTer?
XM_011534464.1:c.1294del XP_011532766.1:p.Arg432AlafsTer?
XM_011534465.1:c.883del XP_011532767.1:p.Arg295AlafsTer?
XR_941090.1:n.1246del
NM_001354984.1:c.1201del NP_001341913.1:p.Arg401AlafsTer?
NM_213647.3:c.1201del MANE Select NP_998812.1:p.Arg401AlafsTer?
NM_001291980.2:c.1097+104del NP_001278909.1:n.1097+104del
NM_001354984.2:c.1201del NP_001341913.1:p.Arg401AlafsTer?
NM_002011.5:c.1201del NP_002002.3:p.Arg401AlafsTer?