Canonical Allele Identifier: CA2321504102

Gene: ADAMTS10

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8600818_8600828delinsCTGTCCCCACG , CM000681.2:g.8600818_8600828delinsCTGTCCCCACG	GRCh38
NC_000019.9:g.8665702_8665712delinsCTGTCCCCACG , CM000681.1:g.8665702_8665712delinsCTGTCCCCACG	GRCh37
NC_000019.8:g.8571702_8571712delinsCTGTCCCCACG	NCBI36
NG_011840.2:g.14875_14885delinsCGTGGGGACAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.810+100_810+110delinsCGTGGGGACAG MANE Select	ENSP00000471851.1:n.810+100_810+110delinsCGTGGGGACAG
ENST00000270328.8:c.810+100_810+110delinsCGTGGGGACAG	ENSP00000270328.4:n.810+100_810+110delinsCGTGGGGACAG
ENST00000593913.5:c.810+100_810+110delinsCGTGGGGACAG	ENSP00000469901.1:n.810+100_810+110delinsCGTGGGGACAG
ENST00000596466.2:n.759+100_759+110delinsCGTGGGGACAG
ENST00000596709.5:n.894+100_894+110delinsCGTGGGGACAG
ENST00000596851.5:c.810+100_810+110delinsCGTGGGGACAG	ENSP00000469559.1:n.810+100_810+110delinsCGTGGGGACAG
ENST00000597188.5:c.810+100_810+110delinsCGTGGGGACAG	ENSP00000471851.1:n.810+100_810+110delinsCGTGGGGACAG
NM_030957.3:c.810+100_810+110delinsCGTGGGGACAG	NP_112219.3:n.810+100_810+110delinsCGTGGGGACAG
XM_006722917.2:c.-300+100_-300+110delinsCGTGGGGACAG	XP_006722980.1:n.-300+100_-300+110delinsCGTGGGGACAG
XM_011528331.1:c.810+100_810+110delinsCGTGGGGACAG	XP_011526633.1:n.810+100_810+110delinsCGTGGGGACAG
XM_011528332.1:c.810+100_810+110delinsCGTGGGGACAG	XP_011526634.1:n.810+100_810+110delinsCGTGGGGACAG
XM_011528333.1:c.810+100_810+110delinsCGTGGGGACAG	XP_011526635.1:n.810+100_810+110delinsCGTGGGGACAG
XM_011528334.1:c.810+100_810+110delinsCGTGGGGACAG	XP_011526636.1:n.810+100_810+110delinsCGTGGGGACAG
XR_430156.2:n.1086+100_1086+110delinsCGTGGGGACAG
XR_936208.1:n.1086+100_1086+110delinsCGTGGGGACAG
XR_936209.1:n.1086+100_1086+110delinsCGTGGGGACAG
XM_006722917.3:c.-300+100_-300+110delinsCGTGGGGACAG	XP_006722980.1:n.-300+100_-300+110delinsCGTGGGGACAG
XM_017027338.2:c.810+100_810+110delinsCGTGGGGACAG	XP_016882827.1:n.810+100_810+110delinsCGTGGGGACAG
XR_001753770.1:n.1646+100_1646+110delinsCGTGGGGACAG
NM_030957.4:c.810+100_810+110delinsCGTGGGGACAG MANE Select	NP_112219.3:n.810+100_810+110delinsCGTGGGGACAG