Canonical Allele Identifier: CA2646916190

Gene: CELSR2

Linked Data

• gnomAD v4: 1-109264385-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109264385_109264386insG , CM000663.2:g.109264385_109264386insG	GRCh38
NC_000001.10:g.109807007_109807008insG , CM000663.1:g.109807007_109807008insG	GRCh37
NC_000001.9:g.109608530_109608531insG	NCBI36
NG_052669.1:g.19681_19682insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271332.4:c.5289+20_5289+21insG MANE Select	ENSP00000271332.3:n.5289+20_5289+21insG
ENST00000271332.3:c.5289+20_5289+21insG	ENSP00000271332.3:n.5289+20_5289+21insG
NM_001408.2:c.5289+20_5289+21insG	NP_001399.1:n.5289+20_5289+21insG
XM_005270580.3:c.5289+20_5289+21insG	XP_005270637.1:n.5289+20_5289+21insG
NM_001408.3:c.5289+20_5289+21insG MANE Select	NP_001399.1:n.5289+20_5289+21insG