Canonical Allele Identifier: CA341501316

Gene: CELSR2

Linked Data

• MyVariant Identifiers: chr1:g.109806733G>A (hg19) ; chr1:g.109264111G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109264111G>A , CM000663.2:g.109264111G>A	GRCh38
NC_000001.10:g.109806733G>A , CM000663.1:g.109806733G>A	GRCh37
NC_000001.9:g.109608256G>A	NCBI36
NG_052669.1:g.19407G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271332.4:c.5035G>A MANE Select	ENSP00000271332.3:p.Gly1679Ser
ENST00000271332.3:c.5035G>A	ENSP00000271332.3:p.Gly1679Ser
NM_001408.2:c.5035G>A	NP_001399.1:p.Gly1679Ser
XM_005270580.3:c.5035G>A	XP_005270637.1:p.Gly1679Ser
NM_001408.3:c.5035G>A MANE Select	NP_001399.1:p.Gly1679Ser