Canonical Allele Identifier: CA2515243175
Gene: ADAMTS10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8604969_8604970insTTTCTG , CM000681.2:g.8604969_8604970insTTTCTG GRCh38
NC_000019.9:g.8669854_8669855insTTTCTG , CM000681.1:g.8669854_8669855insTTTCTG GRCh37
NC_000019.8:g.8575854_8575855insTTTCTG NCBI36
NG_011840.2:g.10733_10734insCAGAAA

Transcript Alleles

HGVS Amino-acid change
ENST00000597188.6:c.435+42_435+43insCAGAAA MANE Select ENSP00000471851.1:n.435+42_435+43insCAGAAA
ENST00000270328.8:c.435+42_435+43insCAGAAA ENSP00000270328.4:n.435+42_435+43insCAGAAA
ENST00000593534.1:n.596_597insCAGAAA
ENST00000593913.5:c.435+42_435+43insCAGAAA ENSP00000469901.1:n.435+42_435+43insCAGAAA
ENST00000596466.2:n.384+42_384+43insCAGAAA
ENST00000596709.5:n.519+42_519+43insCAGAAA
ENST00000596851.5:c.435+42_435+43insCAGAAA ENSP00000469559.1:n.435+42_435+43insCAGAAA
ENST00000597188.5:c.435+42_435+43insCAGAAA ENSP00000471851.1:n.435+42_435+43insCAGAAA
NM_030957.3:c.435+42_435+43insCAGAAA NP_112219.3:n.435+42_435+43insCAGAAA
XM_006722917.2:c.-675+42_-675+43insCAGAAA XP_006722980.1:n.-675+42_-675+43insCAGAAA
XM_011528331.1:c.435+42_435+43insCAGAAA XP_011526633.1:n.435+42_435+43insCAGAAA
XM_011528332.1:c.435+42_435+43insCAGAAA XP_011526634.1:n.435+42_435+43insCAGAAA
XM_011528333.1:c.435+42_435+43insCAGAAA XP_011526635.1:n.435+42_435+43insCAGAAA
XM_011528334.1:c.435+42_435+43insCAGAAA XP_011526636.1:n.435+42_435+43insCAGAAA
XR_430156.2:n.711+42_711+43insCAGAAA
XR_936208.1:n.711+42_711+43insCAGAAA
XR_936209.1:n.711+42_711+43insCAGAAA
XM_006722917.3:c.-675+42_-675+43insCAGAAA XP_006722980.1:n.-675+42_-675+43insCAGAAA
XM_017027338.2:c.435+42_435+43insCAGAAA XP_016882827.1:n.435+42_435+43insCAGAAA
XR_001753770.1:n.1271+42_1271+43insCAGAAA
NM_030957.4:c.435+42_435+43insCAGAAA MANE Select NP_112219.3:n.435+42_435+43insCAGAAA