Canonical Allele Identifier: CA1188035021

Gene: CELSR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109264332C= , CM000663.2:g.109264332C=	GRCh38
NC_000001.10:g.109806954C= , CM000663.1:g.109806954C=	GRCh37
NC_000001.9:g.109608477C=	NCBI36
NG_052669.1:g.19628C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271332.4:c.5256C= MANE Select	ENSP00000271332.3:p.Gly1752=
ENST00000271332.3:c.5256C=	ENSP00000271332.3:p.Gly1752=
NM_001408.2:c.5256C=	NP_001399.1:p.Gly1752=
XM_005270580.3:c.5256C=	XP_005270637.1:p.Gly1752=
NM_001408.3:c.5256C= MANE Select	NP_001399.1:p.Gly1752=