Canonical Allele Identifier: CA1188035016
Gene: CELSR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109264318C= , CM000663.2:g.109264318C= GRCh38
NC_000001.10:g.109806940C= , CM000663.1:g.109806940C= GRCh37
NC_000001.9:g.109608463C= NCBI36
NG_052669.1:g.19614C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000271332.4:c.5242C= MANE Select ENSP00000271332.3:p.Pro1748=
ENST00000271332.3:c.5242C= ENSP00000271332.3:p.Pro1748=
NM_001408.2:c.5242C= NP_001399.1:p.Pro1748=
XM_005270580.3:c.5242C= XP_005270637.1:p.Pro1748=
NM_001408.3:c.5242C= MANE Select NP_001399.1:p.Pro1748=