Canonical Allele Identifier: CA2676682116
Gene: FGFR4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177093289_177093290insCCCCCCCTG , CM000667.2:g.177093289_177093290insCCCCCCCTG GRCh38
NC_000005.9:g.176520290_176520291insCCCCCCCTG , CM000667.1:g.176520290_176520291insCCCCCCCTG GRCh37
NC_000005.8:g.176452896_176452897insCCCCCCCTG NCBI36
NG_012067.1:g.11370_11371insCCCCCCCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000292408.9:c.1209_1210insCCCCCCCTG MANE Select ENSP00000292408.4:p.Pro403_Ala404insProProLeu
ENST00000292408.8:c.1209_1210insCCCCCCCTG ENSP00000292408.4:p.Pro403_Ala404insProProLeu
ENST00000393637.5:c.1058-43_1058-42insCCCCCCCTG ENSP00000377254.1:n.1058-43_1058-42insCCCCCCCTG
ENST00000393648.6:c.1097+112_1097+113insCCCCCCCTG ENSP00000377259.2:n.1097+112_1097+113insCCCCCCCTG
ENST00000502906.5:c.1209_1210insCCCCCCCTG ENSP00000424960.1:p.Pro403_Ala404insProProLeu
ENST00000508139.1:n.513_514insCCCCCCCTG
ENST00000511076.1:c.115_116insCCCCCCCTG
NM_001291980.1:c.1097+112_1097+113insCCCCCCCTG NP_001278909.1:n.1097+112_1097+113insCCCCCCCTG
NM_002011.4:c.1209_1210insCCCCCCCTG NP_002002.3:p.Pro403_Ala404insProProLeu
NM_022963.3:c.1058-43_1058-42insCCCCCCCTG NP_075252.2:n.1058-43_1058-42insCCCCCCCTG
NM_213647.2:c.1209_1210insCCCCCCCTG NP_998812.1:p.Pro403_Ala404insProProLeu
XM_005265838.2:c.1209_1210insCCCCCCCTG XP_005265895.1:p.Pro403_Ala404insProProLeu
XM_011534464.1:c.1302_1303insCCCCCCCTG XP_011532766.1:p.Pro434_Ala435insProProLeu
XM_011534465.1:c.891_892insCCCCCCCTG XP_011532767.1:p.Pro297_Ala298insProProLeu
XR_941090.1:n.1254_1255insCCCCCCCTG
NM_001354984.1:c.1209_1210insCCCCCCCTG NP_001341913.1:p.Pro403_Ala404insProProLeu
NM_213647.3:c.1209_1210insCCCCCCCTG MANE Select NP_998812.1:p.Pro403_Ala404insProProLeu
NM_001291980.2:c.1097+112_1097+113insCCCCCCCTG NP_001278909.1:n.1097+112_1097+113insCCCCCCCTG
NM_001354984.2:c.1209_1210insCCCCCCCTG NP_001341913.1:p.Pro403_Ala404insProProLeu
NM_002011.5:c.1209_1210insCCCCCCCTG NP_002002.3:p.Pro403_Ala404insProProLeu