Canonical Allele Identifier: CA2676682100
Gene: FGFR4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177093289_177093290insCCCCCCGTG , CM000667.2:g.177093289_177093290insCCCCCCGTG GRCh38
NC_000005.9:g.176520290_176520291insCCCCCCGTG , CM000667.1:g.176520290_176520291insCCCCCCGTG GRCh37
NC_000005.8:g.176452896_176452897insCCCCCCGTG NCBI36
NG_012067.1:g.11370_11371insCCCCCCGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000292408.9:c.1209_1210insCCCCCCGTG MANE Select ENSP00000292408.4:p.Pro403_Ala404insProProVal
ENST00000292408.8:c.1209_1210insCCCCCCGTG ENSP00000292408.4:p.Pro403_Ala404insProProVal
ENST00000393637.5:c.1058-43_1058-42insCCCCCCGTG ENSP00000377254.1:n.1058-43_1058-42insCCCCCCGTG
ENST00000393648.6:c.1097+112_1097+113insCCCCCCGTG ENSP00000377259.2:n.1097+112_1097+113insCCCCCCGTG
ENST00000502906.5:c.1209_1210insCCCCCCGTG ENSP00000424960.1:p.Pro403_Ala404insProProVal
ENST00000508139.1:n.513_514insCCCCCCGTG
ENST00000511076.1:c.115_116insCCCCCCGTG
NM_001291980.1:c.1097+112_1097+113insCCCCCCGTG NP_001278909.1:n.1097+112_1097+113insCCCCCCGTG
NM_002011.4:c.1209_1210insCCCCCCGTG NP_002002.3:p.Pro403_Ala404insProProVal
NM_022963.3:c.1058-43_1058-42insCCCCCCGTG NP_075252.2:n.1058-43_1058-42insCCCCCCGTG
NM_213647.2:c.1209_1210insCCCCCCGTG NP_998812.1:p.Pro403_Ala404insProProVal
XM_005265838.2:c.1209_1210insCCCCCCGTG XP_005265895.1:p.Pro403_Ala404insProProVal
XM_011534464.1:c.1302_1303insCCCCCCGTG XP_011532766.1:p.Pro434_Ala435insProProVal
XM_011534465.1:c.891_892insCCCCCCGTG XP_011532767.1:p.Pro297_Ala298insProProVal
XR_941090.1:n.1254_1255insCCCCCCGTG
NM_001354984.1:c.1209_1210insCCCCCCGTG NP_001341913.1:p.Pro403_Ala404insProProVal
NM_213647.3:c.1209_1210insCCCCCCGTG MANE Select NP_998812.1:p.Pro403_Ala404insProProVal
NM_001291980.2:c.1097+112_1097+113insCCCCCCGTG NP_001278909.1:n.1097+112_1097+113insCCCCCCGTG
NM_001354984.2:c.1209_1210insCCCCCCGTG NP_001341913.1:p.Pro403_Ala404insProProVal
NM_002011.5:c.1209_1210insCCCCCCGTG NP_002002.3:p.Pro403_Ala404insProProVal