Canonical Allele Identifier: CA2321502241
Gene: ADAMTS10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8597075G= , CM000681.2:g.8597075G= GRCh38
NC_000019.9:g.8661959G= , CM000681.1:g.8661959G= GRCh37
NC_000019.8:g.8567959G= NCBI36
NG_011840.2:g.18628C=

Transcript Alleles

HGVS Amino-acid change
ENST00000597188.6:c.952C= MANE Select ENSP00000471851.1:p.Gln318=
ENST00000270328.8:c.952C= ENSP00000270328.4:p.Gln318=
ENST00000593913.5:c.*78+9C= ENSP00000469901.1:n.*78+9C=
ENST00000596851.5:c.*87C= ENSP00000469559.1:n.*87C=
ENST00000597188.5:c.952C= ENSP00000471851.1:p.Gln318=
ENST00000601163.1:n.147C=
NM_030957.3:c.952C= NP_112219.3:p.Gln318=
XM_006722917.2:c.-153C= XP_006722980.1:n.-153C=
XM_011528331.1:c.952C= XP_011526633.1:p.Gln318=
XM_011528332.1:c.952C= XP_011526634.1:p.Gln318=
XM_011528333.1:c.952C= XP_011526635.1:p.Gln318=
XM_011528334.1:c.952C= XP_011526636.1:p.Gln318=
XR_430156.2:n.1228C=
XR_936208.1:n.1228C=
XR_936209.1:n.1228C=
XM_006722917.3:c.-153C= XP_006722980.1:n.-153C=
XM_017027338.2:c.952C= XP_016882827.1:p.Gln318=
XR_001753770.1:n.1788C=
NM_030957.4:c.952C= MANE Select NP_112219.3:p.Gln318=