Canonical Allele Identifier: CA2646915930
Gene: CELSR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109264044del , CM000663.2:g.109264044del GRCh38
NC_000001.10:g.109806666del , CM000663.1:g.109806666del GRCh37
NC_000001.9:g.109608189del NCBI36
NG_052669.1:g.19340del

Transcript Alleles

HGVS Amino-acid Change
ENST00000271332.4:c.5002-34del MANE Select ENSP00000271332.3:n.5002-34del
ENST00000271332.3:c.5002-34del ENSP00000271332.3:n.5002-34del
NM_001408.2:c.5002-34del NP_001399.1:n.5002-34del
XM_005270580.3:c.5002-34del XP_005270637.1:n.5002-34del
NM_001408.3:c.5002-34del MANE Select NP_001399.1:n.5002-34del