Canonical Allele Identifier: CA2646916155
Gene: CELSR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109264382_109264383insGCCAC , CM000663.2:g.109264382_109264383insGCCAC GRCh38
NC_000001.10:g.109807004_109807005insGCCAC , CM000663.1:g.109807004_109807005insGCCAC GRCh37
NC_000001.9:g.109608527_109608528insGCCAC NCBI36
NG_052669.1:g.19678_19679insGCCAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000271332.4:c.5289+17_5289+18insGCCAC MANE Select ENSP00000271332.3:n.5289+17_5289+18insGCCAC
ENST00000271332.3:c.5289+17_5289+18insGCCAC ENSP00000271332.3:n.5289+17_5289+18insGCCAC
NM_001408.2:c.5289+17_5289+18insGCCAC NP_001399.1:n.5289+17_5289+18insGCCAC
XM_005270580.3:c.5289+17_5289+18insGCCAC XP_005270637.1:n.5289+17_5289+18insGCCAC
NM_001408.3:c.5289+17_5289+18insGCCAC MANE Select NP_001399.1:n.5289+17_5289+18insGCCAC