Canonical Allele Identifier: CA2321502246

Gene: ADAMTS10

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8597088G= , CM000681.2:g.8597088G=	GRCh38
NC_000019.9:g.8661972G= , CM000681.1:g.8661972G=	GRCh37
NC_000019.8:g.8567972G=	NCBI36
NG_011840.2:g.18615C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000597188.6:c.939C= MANE Select	ENSP00000471851.1:p.Ser313=
ENST00000270328.8:c.939C=	ENSP00000270328.4:p.Ser313=
ENST00000593913.5:c.*74C=	ENSP00000469901.1:n.*74C=
ENST00000596851.5:c.*74C=	ENSP00000469559.1:n.*74C=
ENST00000597188.5:c.939C=	ENSP00000471851.1:p.Ser313=
ENST00000601163.1:n.134C=
NM_030957.3:c.939C=	NP_112219.3:p.Ser313=
XM_006722917.2:c.-166C=	XP_006722980.1:n.-166C=
XM_011528331.1:c.939C=	XP_011526633.1:p.Ser313=
XM_011528332.1:c.939C=	XP_011526634.1:p.Ser313=
XM_011528333.1:c.939C=	XP_011526635.1:p.Ser313=
XM_011528334.1:c.939C=	XP_011526636.1:p.Ser313=
XR_430156.2:n.1215C=
XR_936208.1:n.1215C=
XR_936209.1:n.1215C=
XM_006722917.3:c.-166C=	XP_006722980.1:n.-166C=
XM_017027338.2:c.939C=	XP_016882827.1:p.Ser313=
XR_001753770.1:n.1775C=
NM_030957.4:c.939C= MANE Select	NP_112219.3:p.Ser313=