Canonical Allele Identifier: CA505271205

Gene: ADAMTS10

Linked Data

• MyVariant Identifiers: chr19:g.8661969G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8597085G>A , CM000681.2:g.8597085G>A	GRCh38
NC_000019.9:g.8661969G>A , CM000681.1:g.8661969G>A	GRCh37
NC_000019.8:g.8567969G>A	NCBI36
NG_011840.2:g.18618C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000597188.6:c.942C>T MANE Select	ENSP00000471851.1:p.Phe314=
ENST00000270328.8:c.942C>T	ENSP00000270328.4:p.Phe314=
ENST00000593913.5:c.*77C>T	ENSP00000469901.1:n.*77C>T
ENST00000596851.5:c.*77C>T	ENSP00000469559.1:n.*77C>T
ENST00000597188.5:c.942C>T	ENSP00000471851.1:p.Phe314=
ENST00000601163.1:n.137C>T
NM_030957.3:c.942C>T	NP_112219.3:p.Phe314=
XM_006722917.2:c.-163C>T	XP_006722980.1:n.-163C>T
XM_011528331.1:c.942C>T	XP_011526633.1:p.Phe314=
XM_011528332.1:c.942C>T	XP_011526634.1:p.Phe314=
XM_011528333.1:c.942C>T	XP_011526635.1:p.Phe314=
XM_011528334.1:c.942C>T	XP_011526636.1:p.Phe314=
XR_430156.2:n.1218C>T
XR_936208.1:n.1218C>T
XR_936209.1:n.1218C>T
XM_006722917.3:c.-163C>T	XP_006722980.1:n.-163C>T
XM_017027338.2:c.942C>T	XP_016882827.1:p.Phe314=
XR_001753770.1:n.1778C>T
NM_030957.4:c.942C>T MANE Select	NP_112219.3:p.Phe314=