Canonical Allele Identifier: CA403756101

Gene: ADAMTS10

Linked Data

• MyVariant Identifiers: chr19:g.8661970A>T (hg19) ; chr19:g.8597086A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8597086A>T , CM000681.2:g.8597086A>T	GRCh38
NC_000019.9:g.8661970A>T , CM000681.1:g.8661970A>T	GRCh37
NC_000019.8:g.8567970A>T	NCBI36
NG_011840.2:g.18617T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000597188.6:c.941T>A MANE Select	ENSP00000471851.1:p.Phe314Tyr
ENST00000270328.8:c.941T>A	ENSP00000270328.4:p.Phe314Tyr
ENST00000593913.5:c.*76T>A	ENSP00000469901.1:n.*76T>A
ENST00000596851.5:c.*76T>A	ENSP00000469559.1:n.*76T>A
ENST00000597188.5:c.941T>A	ENSP00000471851.1:p.Phe314Tyr
ENST00000601163.1:n.136T>A
NM_030957.3:c.941T>A	NP_112219.3:p.Phe314Tyr
XM_006722917.2:c.-164T>A	XP_006722980.1:n.-164T>A
XM_011528331.1:c.941T>A	XP_011526633.1:p.Phe314Tyr
XM_011528332.1:c.941T>A	XP_011526634.1:p.Phe314Tyr
XM_011528333.1:c.941T>A	XP_011526635.1:p.Phe314Tyr
XM_011528334.1:c.941T>A	XP_011526636.1:p.Phe314Tyr
XR_430156.2:n.1217T>A
XR_936208.1:n.1217T>A
XR_936209.1:n.1217T>A
XM_006722917.3:c.-164T>A	XP_006722980.1:n.-164T>A
XM_017027338.2:c.941T>A	XP_016882827.1:p.Phe314Tyr
XR_001753770.1:n.1777T>A
NM_030957.4:c.941T>A MANE Select	NP_112219.3:p.Phe314Tyr