Canonical Allele Identifier: CA631368877

Gene: ADAMTS10

Linked Data

• gnomAD v2: 19-8665537-C-CTT
• gnomAD v3: 19-8600653-C-CTT
• gnomAD v4: 19-8600653-C-CTT
• MyVariant Identifiers: chr19:g.8665537_8665538insTT (hg19) ; chr19:g.8600653_8600654insTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8600653_8600654insTT , CM000681.2:g.8600653_8600654insTT	GRCh38
NC_000019.9:g.8665537_8665538insTT , CM000681.1:g.8665537_8665538insTT	GRCh37
NC_000019.8:g.8571537_8571538insTT	NCBI36
NG_011840.2:g.15049_15050insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.810+274_810+275insAA MANE Select	ENSP00000471851.1:n.810+274_810+275insAA
ENST00000270328.8:c.810+274_810+275insAA	ENSP00000270328.4:n.810+274_810+275insAA
ENST00000593913.5:c.810+274_810+275insAA	ENSP00000469901.1:n.810+274_810+275insAA
ENST00000596466.2:n.759+274_759+275insAA
ENST00000596709.5:n.894+274_894+275insAA
ENST00000596851.5:c.810+274_810+275insAA	ENSP00000469559.1:n.810+274_810+275insAA
ENST00000597188.5:c.810+274_810+275insAA	ENSP00000471851.1:n.810+274_810+275insAA
NM_030957.3:c.810+274_810+275insAA	NP_112219.3:n.810+274_810+275insAA
XM_006722917.2:c.-300+274_-300+275insAA	XP_006722980.1:n.-300+274_-300+275insAA
XM_011528331.1:c.810+274_810+275insAA	XP_011526633.1:n.810+274_810+275insAA
XM_011528332.1:c.810+274_810+275insAA	XP_011526634.1:n.810+274_810+275insAA
XM_011528333.1:c.810+274_810+275insAA	XP_011526635.1:n.810+274_810+275insAA
XM_011528334.1:c.810+274_810+275insAA	XP_011526636.1:n.810+274_810+275insAA
XR_430156.2:n.1086+274_1086+275insAA
XR_936208.1:n.1086+274_1086+275insAA
XR_936209.1:n.1086+274_1086+275insAA
XM_006722917.3:c.-300+274_-300+275insAA	XP_006722980.1:n.-300+274_-300+275insAA
XM_017027338.2:c.810+274_810+275insAA	XP_016882827.1:n.810+274_810+275insAA
XR_001753770.1:n.1646+274_1646+275insAA
NM_030957.4:c.810+274_810+275insAA MANE Select	NP_112219.3:n.810+274_810+275insAA