Canonical Allele Identifier: CA9160861
Community Standard Title: NM_030957.4(ADAMTS10):c.401G= (p.Ser134=)
Gene: ADAMTS10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8605046C= , CM000681.2:g.8605046C= GRCh38
NG_011840.2:g.10657G=

Transcript Alleles

HGVS Amino-acid Change
NM_030957.4:c.401G= MANE Select NP_112219.3:p.Ser134=
ENST00000597188.6:c.401G= MANE Select ENSP00000471851.1:p.Ser134=
NM_030957.3:c.401G= NP_112219.3:p.Ser134=
ENST00000270328.8:c.401G= ENSP00000270328.4:p.Ser134=
ENST00000593534.1:n.520G=
ENST00000593913.5:c.401G= ENSP00000469901.1:p.Ser134=
ENST00000596466.2:n.350G=
ENST00000596709.5:n.485G=
ENST00000596851.5:c.401G= ENSP00000469559.1:p.Ser134=
ENST00000597188.5:c.401G= ENSP00000471851.1:p.Ser134=
XM_006722917.2:c.-709G= XP_006722980.1:n.-709G=
XM_006722917.3:c.-709G= XP_006722980.1:n.-709G=
XM_011528331.1:c.401G= XP_011526633.1:p.Ser134=
XM_011528332.1:c.401G= XP_011526634.1:p.Ser134=
XM_011528333.1:c.401G= XP_011526635.1:p.Ser134=
XM_011528334.1:c.401G= XP_011526636.1:p.Ser134=
XM_017027338.2:c.401G= XP_016882827.1:p.Ser134=
XR_001753770.1:n.1237G=
XR_430156.2:n.677G=
XR_936208.1:n.677G=
XR_936209.1:n.677G=