Canonical Allele Identifier: CA1084798805
Gene: FGFR4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177093299_177093303del , CM000667.2:g.177093299_177093303del GRCh38
NC_000005.9:g.176520300_176520304del , CM000667.1:g.176520300_176520304del GRCh37
NC_000005.8:g.176452906_176452910del NCBI36
NG_012067.1:g.11380_11384del

Transcript Alleles

HGVS Amino-acid Change
ENST00000292408.9:c.1219_1223del MANE Select ENSP00000292408.4:p.Gln407AlafsTer?
ENST00000292408.8:c.1219_1223del ENSP00000292408.4:p.Gln407AlafsTer?
ENST00000393637.5:c.1058-33_1058-29del ENSP00000377254.1:n.1058-33_1058-29del
ENST00000393648.6:c.1098-107_1098-103del ENSP00000377259.2:n.1098-107_1098-103del
ENST00000502906.5:c.1219_1223del ENSP00000424960.1:p.Gln407AlafsTer?
ENST00000508139.1:n.523_527del
ENST00000511076.1:c.125_129del
NM_001291980.1:c.1098-107_1098-103del NP_001278909.1:n.1098-107_1098-103del
NM_002011.4:c.1219_1223del NP_002002.3:p.Gln407AlafsTer?
NM_022963.3:c.1058-33_1058-29del NP_075252.2:n.1058-33_1058-29del
NM_213647.2:c.1219_1223del NP_998812.1:p.Gln407AlafsTer?
XM_005265838.2:c.1219_1223del XP_005265895.1:p.Gln407AlafsTer?
XM_011534464.1:c.1312_1316del XP_011532766.1:p.Gln438AlafsTer?
XM_011534465.1:c.901_905del XP_011532767.1:p.Gln301AlafsTer?
XR_941090.1:n.1264_1268del
NM_001354984.1:c.1219_1223del NP_001341913.1:p.Gln407AlafsTer?
NM_213647.3:c.1219_1223del MANE Select NP_998812.1:p.Gln407AlafsTer?
NM_001291980.2:c.1098-107_1098-103del NP_001278909.1:n.1098-107_1098-103del
NM_001354984.2:c.1219_1223del NP_001341913.1:p.Gln407AlafsTer?
NM_002011.5:c.1219_1223del NP_002002.3:p.Gln407AlafsTer?