Canonical Allele Identifier: CA2321505890
Gene: ADAMTS10 HGNC NCBI

Linked Data

dbSNP Id: rs2042702823
gnomAD v4: 19-8604951-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8604951G>A , CM000681.2:g.8604951G>A GRCh38
NC_000019.9:g.8669836G>A , CM000681.1:g.8669836G>A GRCh37
NC_000019.8:g.8575836G>A NCBI36
NG_011840.2:g.10752C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000597188.6:c.435+61C>T MANE Select ENSP00000471851.1:n.435+61C>T
ENST00000270328.8:c.435+61C>T ENSP00000270328.4:n.435+61C>T
ENST00000593534.1:n.615C>T
ENST00000593913.5:c.435+61C>T ENSP00000469901.1:n.435+61C>T
ENST00000596466.2:n.384+61C>T
ENST00000596709.5:n.519+61C>T
ENST00000596851.5:c.435+61C>T ENSP00000469559.1:n.435+61C>T
ENST00000597188.5:c.435+61C>T ENSP00000471851.1:n.435+61C>T
NM_030957.3:c.435+61C>T NP_112219.3:n.435+61C>T
XM_006722917.2:c.-675+61C>T XP_006722980.1:n.-675+61C>T
XM_011528331.1:c.435+61C>T XP_011526633.1:n.435+61C>T
XM_011528332.1:c.435+61C>T XP_011526634.1:n.435+61C>T
XM_011528333.1:c.435+61C>T XP_011526635.1:n.435+61C>T
XM_011528334.1:c.435+61C>T XP_011526636.1:n.435+61C>T
XR_430156.2:n.711+61C>T
XR_936208.1:n.711+61C>T
XR_936209.1:n.711+61C>T
XM_006722917.3:c.-675+61C>T XP_006722980.1:n.-675+61C>T
XM_017027338.2:c.435+61C>T XP_016882827.1:n.435+61C>T
XR_001753770.1:n.1271+61C>T
NM_030957.4:c.435+61C>T MANE Select NP_112219.3:n.435+61C>T