Canonical Allele Identifier: CA403756089
Gene: ADAMTS10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8597081T>G , CM000681.2:g.8597081T>G GRCh38
NC_000019.9:g.8661965T>G , CM000681.1:g.8661965T>G GRCh37
NC_000019.8:g.8567965T>G NCBI36
NG_011840.2:g.18622A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000597188.6:c.946A>C MANE Select ENSP00000471851.1:p.Lys316Gln
ENST00000270328.8:c.946A>C ENSP00000270328.4:p.Lys316Gln
ENST00000593913.5:c.*78+3A>C ENSP00000469901.1:n.*78+3A>C
ENST00000596851.5:c.*81A>C ENSP00000469559.1:n.*81A>C
ENST00000597188.5:c.946A>C ENSP00000471851.1:p.Lys316Gln
ENST00000601163.1:n.141A>C
NM_030957.3:c.946A>C NP_112219.3:p.Lys316Gln
XM_006722917.2:c.-159A>C XP_006722980.1:n.-159A>C
XM_011528331.1:c.946A>C XP_011526633.1:p.Lys316Gln
XM_011528332.1:c.946A>C XP_011526634.1:p.Lys316Gln
XM_011528333.1:c.946A>C XP_011526635.1:p.Lys316Gln
XM_011528334.1:c.946A>C XP_011526636.1:p.Lys316Gln
XR_430156.2:n.1222A>C
XR_936208.1:n.1222A>C
XR_936209.1:n.1222A>C
XM_006722917.3:c.-159A>C XP_006722980.1:n.-159A>C
XM_017027338.2:c.946A>C XP_016882827.1:p.Lys316Gln
XR_001753770.1:n.1782A>C
NM_030957.4:c.946A>C MANE Select NP_112219.3:p.Lys316Gln