Canonical Allele Identifier: CA2676682078
Gene: FGFR4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177093281_177093282insCCCCCCCCCCC , CM000667.2:g.177093281_177093282insCCCCCCCCCCC GRCh38
NC_000005.9:g.176520282_176520283insCCCCCCCCCCC , CM000667.1:g.176520282_176520283insCCCCCCCCCCC GRCh37
NC_000005.8:g.176452888_176452889insCCCCCCCCCCC NCBI36
NG_012067.1:g.11362_11363insCCCCCCCCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000292408.9:c.1201_1202insCCCCCCCCCCC MANE Select ENSP00000292408.4:p.Arg401ProfsTer?
ENST00000292408.8:c.1201_1202insCCCCCCCCCCC ENSP00000292408.4:p.Arg401ProfsTer?
ENST00000393637.5:c.1058-51_1058-50insCCCCCCCCCCC ENSP00000377254.1:n.1058-51_1058-50insCCCCCCCCCCC
ENST00000393648.6:c.1097+104_1097+105insCCCCCCCCCCC ENSP00000377259.2:n.1097+104_1097+105insCCCCCCCCCCC
ENST00000502906.5:c.1201_1202insCCCCCCCCCCC ENSP00000424960.1:p.Arg401ProfsTer?
ENST00000508139.1:n.505_506insCCCCCCCCCCC
ENST00000511076.1:c.107_108insCCCCCCCCCCC
NM_001291980.1:c.1097+104_1097+105insCCCCCCCCCCC NP_001278909.1:n.1097+104_1097+105insCCCCCCCCCCC
NM_002011.4:c.1201_1202insCCCCCCCCCCC NP_002002.3:p.Arg401ProfsTer?
NM_022963.3:c.1058-51_1058-50insCCCCCCCCCCC NP_075252.2:n.1058-51_1058-50insCCCCCCCCCCC
NM_213647.2:c.1201_1202insCCCCCCCCCCC NP_998812.1:p.Arg401ProfsTer?
XM_005265838.2:c.1201_1202insCCCCCCCCCCC XP_005265895.1:p.Arg401ProfsTer?
XM_011534464.1:c.1294_1295insCCCCCCCCCCC XP_011532766.1:p.Arg432ProfsTer?
XM_011534465.1:c.883_884insCCCCCCCCCCC XP_011532767.1:p.Arg295ProfsTer?
XR_941090.1:n.1246_1247insCCCCCCCCCCC
NM_001354984.1:c.1201_1202insCCCCCCCCCCC NP_001341913.1:p.Arg401ProfsTer?
NM_213647.3:c.1201_1202insCCCCCCCCCCC MANE Select NP_998812.1:p.Arg401ProfsTer?
NM_001291980.2:c.1097+104_1097+105insCCCCCCCCCCC NP_001278909.1:n.1097+104_1097+105insCCCCCCCCCCC
NM_001354984.2:c.1201_1202insCCCCCCCCCCC NP_001341913.1:p.Arg401ProfsTer?
NM_002011.5:c.1201_1202insCCCCCCCCCCC NP_002002.3:p.Arg401ProfsTer?