Canonical Allele Identifier: CA1146563353

Gene: CELSR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109264329C= , CM000663.2:g.109264329C=	GRCh38
NC_000001.10:g.109806951C= , CM000663.1:g.109806951C=	GRCh37
NC_000001.9:g.109608474C=	NCBI36
NG_052669.1:g.19625C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271332.4:c.5253C= MANE Select	ENSP00000271332.3:p.Ala1751=
ENST00000271332.3:c.5253C=	ENSP00000271332.3:p.Ala1751=
NM_001408.2:c.5253C=	NP_001399.1:p.Ala1751=
XM_005270580.3:c.5253C=	XP_005270637.1:p.Ala1751=
NM_001408.3:c.5253C= MANE Select	NP_001399.1:p.Ala1751=