Canonical Allele Identifier: CA305002114

Gene: ADAMTS10

Linked Data

• dbSNP Id: rs1027263770
• gnomAD v4: 19-8600936-T-C
• MyVariant Identifiers: chr19:g.8665820T>C (hg19) ; chr19:g.8600936T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8600936T>C , CM000681.2:g.8600936T>C	GRCh38
NC_000019.9:g.8665820T>C , CM000681.1:g.8665820T>C	GRCh37
NC_000019.8:g.8571820T>C	NCBI36
NG_011840.2:g.14767A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000597188.6:c.802A>G MANE Select	ENSP00000471851.1:p.Met268Val
ENST00000270328.8:c.802A>G	ENSP00000270328.4:p.Met268Val
ENST00000593913.5:c.802A>G	ENSP00000469901.1:p.Met268Val
ENST00000596466.2:n.751A>G
ENST00000596709.5:n.886A>G
ENST00000596851.5:c.802A>G	ENSP00000469559.1:p.Met268Val
ENST00000597188.5:c.802A>G	ENSP00000471851.1:p.Met268Val
NM_030957.3:c.802A>G	NP_112219.3:p.Met268Val
XM_006722917.2:c.-308A>G	XP_006722980.1:n.-308A>G
XM_011528331.1:c.802A>G	XP_011526633.1:p.Met268Val
XM_011528332.1:c.802A>G	XP_011526634.1:p.Met268Val
XM_011528333.1:c.802A>G	XP_011526635.1:p.Met268Val
XM_011528334.1:c.802A>G	XP_011526636.1:p.Met268Val
XR_430156.2:n.1078A>G
XR_936208.1:n.1078A>G
XR_936209.1:n.1078A>G
XM_006722917.3:c.-308A>G	XP_006722980.1:n.-308A>G
XM_017027338.2:c.802A>G	XP_016882827.1:p.Met268Val
XR_001753770.1:n.1638A>G
NM_030957.4:c.802A>G MANE Select	NP_112219.3:p.Met268Val