Canonical Allele Identifier: CA2321503954

Gene: ADAMTS10

Linked Data

• dbSNP Id: rs1372856593

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8600670_8600671del , CM000681.2:g.8600670_8600671del	GRCh38
NC_000019.9:g.8665554_8665555del , CM000681.1:g.8665554_8665555del	GRCh37
NC_000019.8:g.8571554_8571555del	NCBI36
NG_011840.2:g.15036_15037del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.810+261_810+262del MANE Select	ENSP00000471851.1:n.810+261_810+262del
ENST00000270328.8:c.810+261_810+262del	ENSP00000270328.4:n.810+261_810+262del
ENST00000593913.5:c.810+261_810+262del	ENSP00000469901.1:n.810+261_810+262del
ENST00000596466.2:n.759+261_759+262del
ENST00000596709.5:n.894+261_894+262del
ENST00000596851.5:c.810+261_810+262del	ENSP00000469559.1:n.810+261_810+262del
ENST00000597188.5:c.810+261_810+262del	ENSP00000471851.1:n.810+261_810+262del
NM_030957.3:c.810+261_810+262del	NP_112219.3:n.810+261_810+262del
XM_006722917.2:c.-300+261_-300+262del	XP_006722980.1:n.-300+261_-300+262del
XM_011528331.1:c.810+261_810+262del	XP_011526633.1:n.810+261_810+262del
XM_011528332.1:c.810+261_810+262del	XP_011526634.1:n.810+261_810+262del
XM_011528333.1:c.810+261_810+262del	XP_011526635.1:n.810+261_810+262del
XM_011528334.1:c.810+261_810+262del	XP_011526636.1:n.810+261_810+262del
XR_430156.2:n.1086+261_1086+262del
XR_936208.1:n.1086+261_1086+262del
XR_936209.1:n.1086+261_1086+262del
XM_006722917.3:c.-300+261_-300+262del	XP_006722980.1:n.-300+261_-300+262del
XM_017027338.2:c.810+261_810+262del	XP_016882827.1:n.810+261_810+262del
XR_001753770.1:n.1646+261_1646+262del
NM_030957.4:c.810+261_810+262del MANE Select	NP_112219.3:n.810+261_810+262del