Canonical Allele Identifier: CA2646916298
Gene: CELSR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109264395_109264396insCCCCCCCAGCAG , CM000663.2:g.109264395_109264396insCCCCCCCAGCAG GRCh38
NC_000001.10:g.109807017_109807018insCCCCCCCAGCAG , CM000663.1:g.109807017_109807018insCCCCCCCAGCAG GRCh37
NC_000001.9:g.109608540_109608541insCCCCCCCAGCAG NCBI36
NG_052669.1:g.19691_19692insCCCCCCCAGCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000271332.4:c.5289+30_5289+31insCCCCCCCAGCAG MANE Select ENSP00000271332.3:n.5289+30_5289+31insCCCCCCCAGCAG
ENST00000271332.3:c.5289+30_5289+31insCCCCCCCAGCAG ENSP00000271332.3:n.5289+30_5289+31insCCCCCCCAGCAG
NM_001408.2:c.5289+30_5289+31insCCCCCCCAGCAG NP_001399.1:n.5289+30_5289+31insCCCCCCCAGCAG
XM_005270580.3:c.5289+30_5289+31insCCCCCCCAGCAG XP_005270637.1:n.5289+30_5289+31insCCCCCCCAGCAG
NM_001408.3:c.5289+30_5289+31insCCCCCCCAGCAG MANE Select NP_001399.1:n.5289+30_5289+31insCCCCCCCAGCAG