Canonical Allele Identifier: CA403748085

Gene: ADAMTS10

Linked Data

• dbSNP Id: rs1555736418
• gnomAD v4: 19-8584913-G-C
• MyVariant Identifiers: chr19:g.8649797G>C (hg19) ; chr19:g.8584913G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8584913G>C , CM000681.2:g.8584913G>C	GRCh38
NC_000019.9:g.8649797G>C , CM000681.1:g.8649797G>C	GRCh37
NC_000019.8:g.8555797G>C	NCBI36
NG_011840.2:g.30790C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000597188.6:c.3184C>G MANE Select	ENSP00000471851.1:p.Pro1062Ala
ENST00000270328.8:c.3184C>G	ENSP00000270328.4:p.Pro1062Ala
ENST00000593913.5:c.*2061C>G	ENSP00000469901.1:n.*2061C>G
ENST00000595838.5:c.1645C>G	ENSP00000470501.1:p.Pro549Ala
ENST00000597188.5:c.3184C>G	ENSP00000471851.1:p.Pro1062Ala
NM_001282352.1:c.1645C>G	NP_001269281.1:p.Pro549Ala
NM_030957.3:c.3184C>G	NP_112219.3:p.Pro1062Ala
XM_006722917.2:c.2227C>G	XP_006722980.1:p.Pro743Ala
XM_011528331.1:c.3331C>G	XP_011526633.1:p.Pro1111Ala
XM_011528332.1:c.3331C>G	XP_011526634.1:p.Pro1111Ala
XM_011528333.1:c.3331C>G	XP_011526635.1:p.Pro1111Ala
XM_011528334.1:c.3007C>G	XP_011526636.1:p.Pro1003Ala
XM_011528335.1:c.1900C>G	XP_011526637.1:p.Pro634Ala
XM_011528336.1:c.1894C>G	XP_011526638.1:p.Pro632Ala
XM_006722917.3:c.2227C>G	XP_006722980.1:p.Pro743Ala
XM_017027338.2:c.3184C>G	XP_016882827.1:p.Pro1062Ala
XM_017027339.1:c.1753C>G	XP_016882828.1:p.Pro585Ala
XM_017027340.1:c.1747C>G	XP_016882829.1:p.Pro583Ala
NM_030957.4:c.3184C>G MANE Select	NP_112219.3:p.Pro1062Ala
NM_001282352.2:c.1645C>G	NP_001269281.1:p.Pro549Ala