Canonical Allele Identifier: CA1142186569
Gene: CELSR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109264549C= , CM000663.2:g.109264549C= GRCh38
NC_000001.10:g.109807171C= , CM000663.1:g.109807171C= GRCh37
NC_000001.9:g.109608694C= NCBI36
NG_052669.1:g.19845C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000271332.4:c.5385C= MANE Select ENSP00000271332.3:p.Asp1795=
ENST00000271332.3:c.5385C= ENSP00000271332.3:p.Asp1795=
NM_001408.2:c.5385C= NP_001399.1:p.Asp1795=
XM_005270580.3:c.5385C= XP_005270637.1:p.Asp1795=
NM_001408.3:c.5385C= MANE Select NP_001399.1:p.Asp1795=