Canonical Allele Identifier: CA1188034943

Gene: CELSR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109264105G= , CM000663.2:g.109264105G=	GRCh38
NC_000001.10:g.109806727G= , CM000663.1:g.109806727G=	GRCh37
NC_000001.9:g.109608250G=	NCBI36
NG_052669.1:g.19401G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271332.4:c.5029G= MANE Select	ENSP00000271332.3:p.Val1677=
ENST00000271332.3:c.5029G=	ENSP00000271332.3:p.Val1677=
NM_001408.2:c.5029G=	NP_001399.1:p.Val1677=
XM_005270580.3:c.5029G=	XP_005270637.1:p.Val1677=
NM_001408.3:c.5029G= MANE Select	NP_001399.1:p.Val1677=