Canonical Allele Identifier: CA973398442
Gene: ADAMTS17 HGNC NCBI

Linked Data

dbSNP Id: rs2060242639

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.99972996_99973015dup , CM000677.2:g.99972996_99973015dup GRCh38
NC_000015.9:g.100513201_100513220dup , CM000677.1:g.100513201_100513220dup GRCh37
NC_000015.8:g.98330724_98330743dup NCBI36
NG_016287.1:g.373965_373984dup
NG_016287.2:g.373965_373984dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000268070.9:c.*1388_*1407dup MANE Select ENSP00000268070.4:n.*1388_*1407dup
ENST00000268070.8:c.*1388_*1407dup ENSP00000268070.4:n.*1388_*1407dup
ENST00000557896.1:n.1687_1706dup
NM_139057.2:c.*1388_*1407dup NP_620688.2:n.*1388_*1407dup
XM_005254872.2:c.*1388_*1407dup XP_005254929.1:n.*1388_*1407dup
XM_011521312.1:c.*1388_*1407dup XP_011519614.1:n.*1388_*1407dup
XR_429624.2:n.1743+263_1743+282dup
NM_139057.3:c.*1388_*1407dup NP_620688.2:n.*1388_*1407dup
XM_005254872.3:c.*1388_*1407dup XP_005254929.1:n.*1388_*1407dup
XM_011521312.2:c.*1388_*1407dup XP_011519614.1:n.*1388_*1407dup
XM_017021973.2:c.*1388_*1407dup XP_016877462.1:n.*1388_*1407dup
XM_017021975.1:c.*1388_*1407dup XP_016877464.1:n.*1388_*1407dup
XM_017021976.1:c.*1388_*1407dup XP_016877465.1:n.*1388_*1407dup
XM_017021978.1:c.*1388_*1407dup XP_016877467.1:n.*1388_*1407dup
XM_017021979.1:c.*1388_*1407dup XP_016877468.1:n.*1388_*1407dup
XM_017021980.1:c.*1388_*1407dup XP_016877469.1:n.*1388_*1407dup
XM_017021982.1:c.*1388_*1407dup XP_016877471.1:n.*1388_*1407dup
XM_017021983.1:c.*1388_*1407dup XP_016877472.1:n.*1388_*1407dup
NM_139057.4:c.*1388_*1407dup MANE Select NP_620688.2:n.*1388_*1407dup