Canonical Allele Identifier: CA748303105

Gene: ADAMTS5

Linked Data

• dbSNP Id: rs162509
• gnomAD v3: 21-26953456-C-A
• gnomAD v4: 21-26953456-C-A
• MyVariant Identifiers: chr21:g.28325775C>A (hg19) ; chr21:g.26953456C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.26953456C>A , CM000683.2:g.26953456C>A	GRCh38
NC_000021.8:g.28325775C>A , CM000683.1:g.28325775C>A	GRCh37
NC_000021.7:g.27247646C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000284987.6:c.1237+1283G>T MANE Select	ENSP00000284987.5:n.1237+1283G>T
ENST00000652031.1:c.419+1283G>T
ENST00000284987.5:c.1237+1283G>T	ENSP00000284987.5:n.1237+1283G>T
NM_007038.3:c.1237+1283G>T	NP_008969.2:n.1237+1283G>T
XM_011529448.1:c.1237+1283G>T	XP_011527750.1:n.1237+1283G>T
NM_007038.4:c.1237+1283G>T	NP_008969.2:n.1237+1283G>T
XM_024452053.1:c.1237+1283G>T	XP_024307821.1:n.1237+1283G>T
XM_024452054.1:c.1237+1283G>T	XP_024307822.1:n.1237+1283G>T
NM_007038.5:c.1237+1283G>T MANE Select	NP_008969.2:n.1237+1283G>T