Canonical Allele Identifier: CA2646916383

Gene: CELSR2

Linked Data

• gnomAD v4: 1-109264437-G-GCTC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109264440_109264442dup , CM000663.2:g.109264440_109264442dup	GRCh38
NC_000001.10:g.109807062_109807064dup , CM000663.1:g.109807062_109807064dup	GRCh37
NC_000001.9:g.109608585_109608587dup	NCBI36
NG_052669.1:g.19736_19738dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271332.4:c.5290-14_5290-12dup MANE Select	ENSP00000271332.3:n.5290-14_5290-12dup
ENST00000271332.3:c.5290-14_5290-12dup	ENSP00000271332.3:n.5290-14_5290-12dup
NM_001408.2:c.5290-14_5290-12dup	NP_001399.1:n.5290-14_5290-12dup
XM_005270580.3:c.5290-14_5290-12dup	XP_005270637.1:n.5290-14_5290-12dup
NM_001408.3:c.5290-14_5290-12dup MANE Select	NP_001399.1:n.5290-14_5290-12dup