Canonical Allele Identifier: CA1084798804
Gene: FGFR4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177093289_177093290insCCCCCAGGG , CM000667.2:g.177093289_177093290insCCCCCAGGG GRCh38
NC_000005.9:g.176520290_176520291insCCCCCAGGG , CM000667.1:g.176520290_176520291insCCCCCAGGG GRCh37
NC_000005.8:g.176452896_176452897insCCCCCAGGG NCBI36
NG_012067.1:g.11370_11371insCCCCCAGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000292408.9:c.1209_1210insCCCCCAGGG MANE Select ENSP00000292408.4:p.Pro403_Ala404insProProGly
ENST00000292408.8:c.1209_1210insCCCCCAGGG ENSP00000292408.4:p.Pro403_Ala404insProProGly
ENST00000393637.5:c.1058-43_1058-42insCCCCCAGGG ENSP00000377254.1:n.1058-43_1058-42insCCCCCAGGG
ENST00000393648.6:c.1097+112_1097+113insCCCCCAGGG ENSP00000377259.2:n.1097+112_1097+113insCCCCCAGGG
ENST00000502906.5:c.1209_1210insCCCCCAGGG ENSP00000424960.1:p.Pro403_Ala404insProProGly
ENST00000508139.1:n.513_514insCCCCCAGGG
ENST00000511076.1:c.115_116insCCCCCAGGG
NM_001291980.1:c.1097+112_1097+113insCCCCCAGGG NP_001278909.1:n.1097+112_1097+113insCCCCCAGGG
NM_002011.4:c.1209_1210insCCCCCAGGG NP_002002.3:p.Pro403_Ala404insProProGly
NM_022963.3:c.1058-43_1058-42insCCCCCAGGG NP_075252.2:n.1058-43_1058-42insCCCCCAGGG
NM_213647.2:c.1209_1210insCCCCCAGGG NP_998812.1:p.Pro403_Ala404insProProGly
XM_005265838.2:c.1209_1210insCCCCCAGGG XP_005265895.1:p.Pro403_Ala404insProProGly
XM_011534464.1:c.1302_1303insCCCCCAGGG XP_011532766.1:p.Pro434_Ala435insProProGly
XM_011534465.1:c.891_892insCCCCCAGGG XP_011532767.1:p.Pro297_Ala298insProProGly
XR_941090.1:n.1254_1255insCCCCCAGGG
NM_001354984.1:c.1209_1210insCCCCCAGGG NP_001341913.1:p.Pro403_Ala404insProProGly
NM_213647.3:c.1209_1210insCCCCCAGGG MANE Select NP_998812.1:p.Pro403_Ala404insProProGly
NM_001291980.2:c.1097+112_1097+113insCCCCCAGGG NP_001278909.1:n.1097+112_1097+113insCCCCCAGGG
NM_001354984.2:c.1209_1210insCCCCCAGGG NP_001341913.1:p.Pro403_Ala404insProProGly
NM_002011.5:c.1209_1210insCCCCCAGGG NP_002002.3:p.Pro403_Ala404insProProGly