Canonical Allele Identifier: CA2646915916
Gene: CELSR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109264028_109264029del , CM000663.2:g.109264028_109264029del GRCh38
NC_000001.10:g.109806650_109806651del , CM000663.1:g.109806650_109806651del GRCh37
NC_000001.9:g.109608173_109608174del NCBI36
NG_052669.1:g.19324_19325del

Transcript Alleles

HGVS Amino-acid Change
ENST00000271332.4:c.5002-50_5002-49del MANE Select ENSP00000271332.3:n.5002-50_5002-49del
ENST00000271332.3:c.5002-50_5002-49del ENSP00000271332.3:n.5002-50_5002-49del
NM_001408.2:c.5002-50_5002-49del NP_001399.1:n.5002-50_5002-49del
XM_005270580.3:c.5002-50_5002-49del XP_005270637.1:n.5002-50_5002-49del
NM_001408.3:c.5002-50_5002-49del MANE Select NP_001399.1:n.5002-50_5002-49del