Canonical Allele Identifier: CA884327761

Gene: ADAMTS10

Linked Data

• dbSNP Id: rs1449438961
• gnomAD v3: 19-8600667-T-TG
• gnomAD v4: 19-8600667-T-TG
• MyVariant Identifiers: chr19:g.8600667_8600668insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8600667_8600668insG , CM000681.2:g.8600667_8600668insG	GRCh38
NC_000019.9:g.8665551_8665552insG , CM000681.1:g.8665551_8665552insG	GRCh37
NC_000019.8:g.8571551_8571552insG	NCBI36
NG_011840.2:g.15035_15036insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.810+260_810+261insC MANE Select	ENSP00000471851.1:n.810+260_810+261insC
ENST00000270328.8:c.810+260_810+261insC	ENSP00000270328.4:n.810+260_810+261insC
ENST00000593913.5:c.810+260_810+261insC	ENSP00000469901.1:n.810+260_810+261insC
ENST00000596466.2:n.759+260_759+261insC
ENST00000596709.5:n.894+260_894+261insC
ENST00000596851.5:c.810+260_810+261insC	ENSP00000469559.1:n.810+260_810+261insC
ENST00000597188.5:c.810+260_810+261insC	ENSP00000471851.1:n.810+260_810+261insC
NM_030957.3:c.810+260_810+261insC	NP_112219.3:n.810+260_810+261insC
XM_006722917.2:c.-300+260_-300+261insC	XP_006722980.1:n.-300+260_-300+261insC
XM_011528331.1:c.810+260_810+261insC	XP_011526633.1:n.810+260_810+261insC
XM_011528332.1:c.810+260_810+261insC	XP_011526634.1:n.810+260_810+261insC
XM_011528333.1:c.810+260_810+261insC	XP_011526635.1:n.810+260_810+261insC
XM_011528334.1:c.810+260_810+261insC	XP_011526636.1:n.810+260_810+261insC
XR_430156.2:n.1086+260_1086+261insC
XR_936208.1:n.1086+260_1086+261insC
XR_936209.1:n.1086+260_1086+261insC
XM_006722917.3:c.-300+260_-300+261insC	XP_006722980.1:n.-300+260_-300+261insC
XM_017027338.2:c.810+260_810+261insC	XP_016882827.1:n.810+260_810+261insC
XR_001753770.1:n.1646+260_1646+261insC
NM_030957.4:c.810+260_810+261insC MANE Select	NP_112219.3:n.810+260_810+261insC