Canonical Allele Identifier: CA2321502243

Gene: ADAMTS10

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8597082A= , CM000681.2:g.8597082A=	GRCh38
NC_000019.9:g.8661966A= , CM000681.1:g.8661966A=	GRCh37
NC_000019.8:g.8567966A=	NCBI36
NG_011840.2:g.18621T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000597188.6:c.945T= MANE Select	ENSP00000471851.1:p.Cys315=
ENST00000270328.8:c.945T=	ENSP00000270328.4:p.Cys315=
ENST00000593913.5:c.*78+2T=	ENSP00000469901.1:n.*78+2T=
ENST00000596851.5:c.*80T=	ENSP00000469559.1:n.*80T=
ENST00000597188.5:c.945T=	ENSP00000471851.1:p.Cys315=
ENST00000601163.1:n.140T=
NM_030957.3:c.945T=	NP_112219.3:p.Cys315=
XM_006722917.2:c.-160T=	XP_006722980.1:n.-160T=
XM_011528331.1:c.945T=	XP_011526633.1:p.Cys315=
XM_011528332.1:c.945T=	XP_011526634.1:p.Cys315=
XM_011528333.1:c.945T=	XP_011526635.1:p.Cys315=
XM_011528334.1:c.945T=	XP_011526636.1:p.Cys315=
XR_430156.2:n.1221T=
XR_936208.1:n.1221T=
XR_936209.1:n.1221T=
XM_006722917.3:c.-160T=	XP_006722980.1:n.-160T=
XM_017027338.2:c.945T=	XP_016882827.1:p.Cys315=
XR_001753770.1:n.1781T=
NM_030957.4:c.945T= MANE Select	NP_112219.3:p.Cys315=