Canonical Allele Identifier: CA2676682099
Gene: FGFR4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177093289_177093290insCCCCCCGGT , CM000667.2:g.177093289_177093290insCCCCCCGGT GRCh38
NC_000005.9:g.176520290_176520291insCCCCCCGGT , CM000667.1:g.176520290_176520291insCCCCCCGGT GRCh37
NC_000005.8:g.176452896_176452897insCCCCCCGGT NCBI36
NG_012067.1:g.11370_11371insCCCCCCGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000292408.9:c.1209_1210insCCCCCCGGT MANE Select ENSP00000292408.4:p.Pro403_Ala404insProProGly
ENST00000292408.8:c.1209_1210insCCCCCCGGT ENSP00000292408.4:p.Pro403_Ala404insProProGly
ENST00000393637.5:c.1058-43_1058-42insCCCCCCGGT ENSP00000377254.1:n.1058-43_1058-42insCCCCCCGGT
ENST00000393648.6:c.1097+112_1097+113insCCCCCCGGT ENSP00000377259.2:n.1097+112_1097+113insCCCCCCGGT
ENST00000502906.5:c.1209_1210insCCCCCCGGT ENSP00000424960.1:p.Pro403_Ala404insProProGly
ENST00000508139.1:n.513_514insCCCCCCGGT
ENST00000511076.1:c.115_116insCCCCCCGGT
NM_001291980.1:c.1097+112_1097+113insCCCCCCGGT NP_001278909.1:n.1097+112_1097+113insCCCCCCGGT
NM_002011.4:c.1209_1210insCCCCCCGGT NP_002002.3:p.Pro403_Ala404insProProGly
NM_022963.3:c.1058-43_1058-42insCCCCCCGGT NP_075252.2:n.1058-43_1058-42insCCCCCCGGT
NM_213647.2:c.1209_1210insCCCCCCGGT NP_998812.1:p.Pro403_Ala404insProProGly
XM_005265838.2:c.1209_1210insCCCCCCGGT XP_005265895.1:p.Pro403_Ala404insProProGly
XM_011534464.1:c.1302_1303insCCCCCCGGT XP_011532766.1:p.Pro434_Ala435insProProGly
XM_011534465.1:c.891_892insCCCCCCGGT XP_011532767.1:p.Pro297_Ala298insProProGly
XR_941090.1:n.1254_1255insCCCCCCGGT
NM_001354984.1:c.1209_1210insCCCCCCGGT NP_001341913.1:p.Pro403_Ala404insProProGly
NM_213647.3:c.1209_1210insCCCCCCGGT MANE Select NP_998812.1:p.Pro403_Ala404insProProGly
NM_001291980.2:c.1097+112_1097+113insCCCCCCGGT NP_001278909.1:n.1097+112_1097+113insCCCCCCGGT
NM_001354984.2:c.1209_1210insCCCCCCGGT NP_001341913.1:p.Pro403_Ala404insProProGly
NM_002011.5:c.1209_1210insCCCCCCGGT NP_002002.3:p.Pro403_Ala404insProProGly