Canonical Allele Identifier: CA403756438

Gene: ADAMTS10

Linked Data

• MyVariant Identifiers: chr19:g.8665817T>G (hg19) ; chr19:g.8600933T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8600933T>G , CM000681.2:g.8600933T>G	GRCh38
NC_000019.9:g.8665817T>G , CM000681.1:g.8665817T>G	GRCh37
NC_000019.8:g.8571817T>G	NCBI36
NG_011840.2:g.14770A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000597188.6:c.805A>C MANE Select	ENSP00000471851.1:p.Asn269His
ENST00000270328.8:c.805A>C	ENSP00000270328.4:p.Asn269His
ENST00000593913.5:c.805A>C	ENSP00000469901.1:p.Asn269His
ENST00000596466.2:n.754A>C
ENST00000596709.5:n.889A>C
ENST00000596851.5:c.805A>C	ENSP00000469559.1:p.Asn269His
ENST00000597188.5:c.805A>C	ENSP00000471851.1:p.Asn269His
NM_030957.3:c.805A>C	NP_112219.3:p.Asn269His
XM_006722917.2:c.-305A>C	XP_006722980.1:n.-305A>C
XM_011528331.1:c.805A>C	XP_011526633.1:p.Asn269His
XM_011528332.1:c.805A>C	XP_011526634.1:p.Asn269His
XM_011528333.1:c.805A>C	XP_011526635.1:p.Asn269His
XM_011528334.1:c.805A>C	XP_011526636.1:p.Asn269His
XR_430156.2:n.1081A>C
XR_936208.1:n.1081A>C
XR_936209.1:n.1081A>C
XM_006722917.3:c.-305A>C	XP_006722980.1:n.-305A>C
XM_017027338.2:c.805A>C	XP_016882827.1:p.Asn269His
XR_001753770.1:n.1641A>C
NM_030957.4:c.805A>C MANE Select	NP_112219.3:p.Asn269His