Canonical Allele Identifier: CA1148442087
Gene: CELSR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109264521A= , CM000663.2:g.109264521A= GRCh38
NC_000001.10:g.109807143A= , CM000663.1:g.109807143A= GRCh37
NC_000001.9:g.109608666A= NCBI36
NG_052669.1:g.19817A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000271332.4:c.5357A= MANE Select ENSP00000271332.3:p.Asn1786=
ENST00000271332.3:c.5357A= ENSP00000271332.3:p.Asn1786=
NM_001408.2:c.5357A= NP_001399.1:p.Asn1786=
XM_005270580.3:c.5357A= XP_005270637.1:p.Asn1786=
NM_001408.3:c.5357A= MANE Select NP_001399.1:p.Asn1786=