Canonical Allele Identifier: CA2321502242

Gene: ADAMTS10

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8597076C= , CM000681.2:g.8597076C=	GRCh38
NC_000019.9:g.8661960C= , CM000681.1:g.8661960C=	GRCh37
NC_000019.8:g.8567960C=	NCBI36
NG_011840.2:g.18627G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000597188.6:c.951G= MANE Select	ENSP00000471851.1:p.Trp317=
ENST00000270328.8:c.951G=	ENSP00000270328.4:p.Trp317=
ENST00000593913.5:c.*78+8G=	ENSP00000469901.1:n.*78+8G=
ENST00000596851.5:c.*86G=	ENSP00000469559.1:n.*86G=
ENST00000597188.5:c.951G=	ENSP00000471851.1:p.Trp317=
ENST00000601163.1:n.146G=
NM_030957.3:c.951G=	NP_112219.3:p.Trp317=
XM_006722917.2:c.-154G=	XP_006722980.1:n.-154G=
XM_011528331.1:c.951G=	XP_011526633.1:p.Trp317=
XM_011528332.1:c.951G=	XP_011526634.1:p.Trp317=
XM_011528333.1:c.951G=	XP_011526635.1:p.Trp317=
XM_011528334.1:c.951G=	XP_011526636.1:p.Trp317=
XR_430156.2:n.1227G=
XR_936208.1:n.1227G=
XR_936209.1:n.1227G=
XM_006722917.3:c.-154G=	XP_006722980.1:n.-154G=
XM_017027338.2:c.951G=	XP_016882827.1:p.Trp317=
XR_001753770.1:n.1787G=
NM_030957.4:c.951G= MANE Select	NP_112219.3:p.Trp317=