Canonical Allele Identifier: CA1188034906
Gene: CELSR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109264033_109264034delinsAT , CM000663.2:g.109264033_109264034delinsAT GRCh38
NC_000001.10:g.109806655_109806656delinsAT , CM000663.1:g.109806655_109806656delinsAT GRCh37
NC_000001.9:g.109608178_109608179delinsAT NCBI36
NG_052669.1:g.19329_19330delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000271332.4:c.5002-45_5002-44delinsAT MANE Select ENSP00000271332.3:n.5002-45_5002-44delinsAT
ENST00000271332.3:c.5002-45_5002-44delinsAT ENSP00000271332.3:n.5002-45_5002-44delinsAT
NM_001408.2:c.5002-45_5002-44delinsAT NP_001399.1:n.5002-45_5002-44delinsAT
XM_005270580.3:c.5002-45_5002-44delinsAT XP_005270637.1:n.5002-45_5002-44delinsAT
NM_001408.3:c.5002-45_5002-44delinsAT MANE Select NP_001399.1:n.5002-45_5002-44delinsAT