Canonical Allele Identifier: CA505266494

Gene: ADAMTS10

Linked Data

• gnomAD v4: 19-8584911-G-T
• MyVariant Identifiers: chr19:g.8649795G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8584911G>T , CM000681.2:g.8584911G>T	GRCh38
NC_000019.9:g.8649795G>T , CM000681.1:g.8649795G>T	GRCh37
NC_000019.8:g.8555795G>T	NCBI36
NG_011840.2:g.30792C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000597188.6:c.3186C>A MANE Select	ENSP00000471851.1:p.Pro1062=
ENST00000270328.8:c.3186C>A	ENSP00000270328.4:p.Pro1062=
ENST00000593913.5:c.*2063C>A	ENSP00000469901.1:n.*2063C>A
ENST00000595838.5:c.1647C>A	ENSP00000470501.1:p.Pro549=
ENST00000597188.5:c.3186C>A	ENSP00000471851.1:p.Pro1062=
NM_001282352.1:c.1647C>A	NP_001269281.1:p.Pro549=
NM_030957.3:c.3186C>A	NP_112219.3:p.Pro1062=
XM_006722917.2:c.2229C>A	XP_006722980.1:p.Pro743=
XM_011528331.1:c.3333C>A	XP_011526633.1:p.Pro1111=
XM_011528332.1:c.3333C>A	XP_011526634.1:p.Pro1111=
XM_011528333.1:c.3333C>A	XP_011526635.1:p.Pro1111=
XM_011528334.1:c.3009C>A	XP_011526636.1:p.Pro1003=
XM_011528335.1:c.1902C>A	XP_011526637.1:p.Pro634=
XM_011528336.1:c.1896C>A	XP_011526638.1:p.Pro632=
XM_006722917.3:c.2229C>A	XP_006722980.1:p.Pro743=
XM_017027338.2:c.3186C>A	XP_016882827.1:p.Pro1062=
XM_017027339.1:c.1755C>A	XP_016882828.1:p.Pro585=
XM_017027340.1:c.1749C>A	XP_016882829.1:p.Pro583=
NM_030957.4:c.3186C>A MANE Select	NP_112219.3:p.Pro1062=
NM_001282352.2:c.1647C>A	NP_001269281.1:p.Pro549=