Canonical Allele Identifier: CA2199786998
Gene: ADAMTS17 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.99973030_99973033delinsGTGA , CM000677.2:g.99973030_99973033delinsGTGA GRCh38
NC_000015.9:g.100513235_100513238delinsGTGA , CM000677.1:g.100513235_100513238delinsGTGA GRCh37
NC_000015.8:g.98330758_98330761delinsGTGA NCBI36
NG_016287.1:g.373946_373949delinsTCAC
NG_016287.2:g.373946_373949delinsTCAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000268070.9:c.*1369_*1372delinsTCAC MANE Select ENSP00000268070.4:n.*1369_*1372delinsTCAC
ENST00000268070.8:c.*1369_*1372delinsTCAC ENSP00000268070.4:n.*1369_*1372delinsTCAC
ENST00000557896.1:n.1668_1671delinsTCAC
NM_139057.2:c.*1369_*1372delinsTCAC NP_620688.2:n.*1369_*1372delinsTCAC
XM_005254872.2:c.*1369_*1372delinsTCAC XP_005254929.1:n.*1369_*1372delinsTCAC
XM_011521312.1:c.*1369_*1372delinsTCAC XP_011519614.1:n.*1369_*1372delinsTCAC
XR_429624.2:n.1743+297_1743+300delinsGTGA
NM_139057.3:c.*1369_*1372delinsTCAC NP_620688.2:n.*1369_*1372delinsTCAC
XM_005254872.3:c.*1369_*1372delinsTCAC XP_005254929.1:n.*1369_*1372delinsTCAC
XM_011521312.2:c.*1369_*1372delinsTCAC XP_011519614.1:n.*1369_*1372delinsTCAC
XM_017021973.2:c.*1369_*1372delinsTCAC XP_016877462.1:n.*1369_*1372delinsTCAC
XM_017021975.1:c.*1369_*1372delinsTCAC XP_016877464.1:n.*1369_*1372delinsTCAC
XM_017021976.1:c.*1369_*1372delinsTCAC XP_016877465.1:n.*1369_*1372delinsTCAC
XM_017021978.1:c.*1369_*1372delinsTCAC XP_016877467.1:n.*1369_*1372delinsTCAC
XM_017021979.1:c.*1369_*1372delinsTCAC XP_016877468.1:n.*1369_*1372delinsTCAC
XM_017021980.1:c.*1369_*1372delinsTCAC XP_016877469.1:n.*1369_*1372delinsTCAC
XM_017021982.1:c.*1369_*1372delinsTCAC XP_016877471.1:n.*1369_*1372delinsTCAC
XM_017021983.1:c.*1369_*1372delinsTCAC XP_016877472.1:n.*1369_*1372delinsTCAC
NM_139057.4:c.*1369_*1372delinsTCAC MANE Select NP_620688.2:n.*1369_*1372delinsTCAC