Canonical Allele Identifier: CA2676682084
Gene: FGFR4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177093282del , CM000667.2:g.177093282del GRCh38
NC_000005.9:g.176520283del , CM000667.1:g.176520283del GRCh37
NC_000005.8:g.176452889del NCBI36
NG_012067.1:g.11363del

Transcript Alleles

HGVS Amino-acid Change
ENST00000292408.9:c.1202del MANE Select ENSP00000292408.4:p.Arg401ProfsTer?
ENST00000292408.8:c.1202del ENSP00000292408.4:p.Arg401ProfsTer?
ENST00000393637.5:c.1058-50del ENSP00000377254.1:n.1058-50del
ENST00000393648.6:c.1097+105del ENSP00000377259.2:n.1097+105del
ENST00000502906.5:c.1202del ENSP00000424960.1:p.Arg401ProfsTer?
ENST00000508139.1:n.506del
ENST00000511076.1:c.108del
NM_001291980.1:c.1097+105del NP_001278909.1:n.1097+105del
NM_002011.4:c.1202del NP_002002.3:p.Arg401ProfsTer?
NM_022963.3:c.1058-50del NP_075252.2:n.1058-50del
NM_213647.2:c.1202del NP_998812.1:p.Arg401ProfsTer?
XM_005265838.2:c.1202del XP_005265895.1:p.Arg401ProfsTer?
XM_011534464.1:c.1295del XP_011532766.1:p.Arg432ProfsTer?
XM_011534465.1:c.884del XP_011532767.1:p.Arg295ProfsTer?
XR_941090.1:n.1247del
NM_001354984.1:c.1202del NP_001341913.1:p.Arg401ProfsTer?
NM_213647.3:c.1202del MANE Select NP_998812.1:p.Arg401ProfsTer?
NM_001291980.2:c.1097+105del NP_001278909.1:n.1097+105del
NM_001354984.2:c.1202del NP_001341913.1:p.Arg401ProfsTer?
NM_002011.5:c.1202del NP_002002.3:p.Arg401ProfsTer?