Canonical Allele Identifier: CA1144726123

Gene: CELSR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109264390A= , CM000663.2:g.109264390A=	GRCh38
NC_000001.10:g.109807012A= , CM000663.1:g.109807012A=	GRCh37
NC_000001.9:g.109608535A=	NCBI36
NG_052669.1:g.19686A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271332.4:c.5289+25A= MANE Select	ENSP00000271332.3:n.5289+25A=
ENST00000271332.3:c.5289+25A=	ENSP00000271332.3:n.5289+25A=
NM_001408.2:c.5289+25A=	NP_001399.1:n.5289+25A=
XM_005270580.3:c.5289+25A=	XP_005270637.1:n.5289+25A=
NM_001408.3:c.5289+25A= MANE Select	NP_001399.1:n.5289+25A=