Canonical Allele Identifier: CA631368913

Gene: ADAMTS10

Linked Data

• dbSNP Id: rs1300832524
• gnomAD v2: 19-8665567-A-G
• gnomAD v3: 19-8600683-A-G
• gnomAD v4: 19-8600683-A-G
• MyVariant Identifiers: chr19:g.8665567A>G (hg19) ; chr19:g.8600683A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8600683A>G , CM000681.2:g.8600683A>G	GRCh38
NC_000019.9:g.8665567A>G , CM000681.1:g.8665567A>G	GRCh37
NC_000019.8:g.8571567A>G	NCBI36
NG_011840.2:g.15020T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.810+245T>C MANE Select	ENSP00000471851.1:n.810+245T>C
ENST00000270328.8:c.810+245T>C	ENSP00000270328.4:n.810+245T>C
ENST00000593913.5:c.810+245T>C	ENSP00000469901.1:n.810+245T>C
ENST00000596466.2:n.759+245T>C
ENST00000596709.5:n.894+245T>C
ENST00000596851.5:c.810+245T>C	ENSP00000469559.1:n.810+245T>C
ENST00000597188.5:c.810+245T>C	ENSP00000471851.1:n.810+245T>C
NM_030957.3:c.810+245T>C	NP_112219.3:n.810+245T>C
XM_006722917.2:c.-300+245T>C	XP_006722980.1:n.-300+245T>C
XM_011528331.1:c.810+245T>C	XP_011526633.1:n.810+245T>C
XM_011528332.1:c.810+245T>C	XP_011526634.1:n.810+245T>C
XM_011528333.1:c.810+245T>C	XP_011526635.1:n.810+245T>C
XM_011528334.1:c.810+245T>C	XP_011526636.1:n.810+245T>C
XR_430156.2:n.1086+245T>C
XR_936208.1:n.1086+245T>C
XR_936209.1:n.1086+245T>C
XM_006722917.3:c.-300+245T>C	XP_006722980.1:n.-300+245T>C
XM_017027338.2:c.810+245T>C	XP_016882827.1:n.810+245T>C
XR_001753770.1:n.1646+245T>C
NM_030957.4:c.810+245T>C MANE Select	NP_112219.3:n.810+245T>C