Canonical Allele Identifier: CA403755888

Gene: ADAMTS10

Linked Data

• MyVariant Identifiers: chr19:g.8661876G>C (hg19) ; chr19:g.8596992G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8596992G>C , CM000681.2:g.8596992G>C	GRCh38
NC_000019.9:g.8661876G>C , CM000681.1:g.8661876G>C	GRCh37
NC_000019.8:g.8567876G>C	NCBI36
NG_011840.2:g.18711C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.1035C>G MANE Select	ENSP00000471851.1:p.Ile345Met
ENST00000270328.8:c.1035C>G	ENSP00000270328.4:p.Ile345Met
ENST00000593913.5:c.*78+92C>G	ENSP00000469901.1:n.*78+92C>G
ENST00000596851.5:c.*170C>G	ENSP00000469559.1:n.*170C>G
ENST00000597188.5:c.1035C>G	ENSP00000471851.1:p.Ile345Met
ENST00000601163.1:n.230C>G
NM_030957.3:c.1035C>G	NP_112219.3:p.Ile345Met
XM_006722917.2:c.-70C>G	XP_006722980.1:n.-70C>G
XM_011528331.1:c.1035C>G	XP_011526633.1:p.Ile345Met
XM_011528332.1:c.1035C>G	XP_011526634.1:p.Ile345Met
XM_011528333.1:c.1035C>G	XP_011526635.1:p.Ile345Met
XM_011528334.1:c.1035C>G	XP_011526636.1:p.Ile345Met
XR_430156.2:n.1311C>G
XR_936208.1:n.1311C>G
XR_936209.1:n.1311C>G
XM_006722917.3:c.-70C>G	XP_006722980.1:n.-70C>G
XM_017027338.2:c.1035C>G	XP_016882827.1:p.Ile345Met
XR_001753770.1:n.1871C>G
NM_030957.4:c.1035C>G MANE Select	NP_112219.3:p.Ile345Met