Canonical Allele Identifier: CA645586467
Gene: ADAMTS17 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.100132005_100132006insG , CM000677.2:g.100132005_100132006insG GRCh38
NC_000015.9:g.100672210_100672211insG , CM000677.1:g.100672210_100672211insG GRCh37
NC_000015.8:g.98489733_98489734insG NCBI36
NG_016287.1:g.214973_214974insC
NG_016287.2:g.214973_214974insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000268070.9:c.1721+1_1721+2insC MANE Select ENSP00000268070.4:n.1721+1_1721+2insC
ENST00000568565.2:c.1721+1_1721+2insC ENSP00000456161.2:n.1721+1_1721+2insC
ENST00000268070.8:c.1721+1_1721+2insC ENSP00000268070.4:n.1721+1_1721+2insC
ENST00000378898.8:n.1402+1_1402+2insC
NM_139057.2:c.1721+1_1721+2insC NP_620688.2:n.1721+1_1721+2insC
XM_005254872.2:c.1721+1_1721+2insC XP_005254929.1:n.1721+1_1721+2insC
XM_011521312.1:c.1721+1_1721+2insC XP_011519614.1:n.1721+1_1721+2insC
NM_139057.3:c.1721+1_1721+2insC NP_620688.2:n.1721+1_1721+2insC
XM_005254872.3:c.1721+1_1721+2insC XP_005254929.1:n.1721+1_1721+2insC
XM_011521312.2:c.1721+1_1721+2insC XP_011519614.1:n.1721+1_1721+2insC
XM_017021973.2:c.1853+1_1853+2insC XP_016877462.1:n.1853+1_1853+2insC
XM_017021974.1:c.1853+1_1853+2insC XP_016877463.1:n.1853+1_1853+2insC
XM_017021975.1:c.1853+1_1853+2insC XP_016877464.1:n.1853+1_1853+2insC
XM_017021976.1:c.1124+1_1124+2insC XP_016877465.1:n.1124+1_1124+2insC
XM_017021977.1:c.1853+1_1853+2insC XP_016877466.1:n.1853+1_1853+2insC
XM_017021978.1:c.755+1_755+2insC XP_016877467.1:n.755+1_755+2insC
XM_017021979.1:c.533+1_533+2insC XP_016877468.1:n.533+1_533+2insC
XM_017021980.1:c.533+1_533+2insC XP_016877469.1:n.533+1_533+2insC
XM_017021981.1:c.1853+1_1853+2insC XP_016877470.1:n.1853+1_1853+2insC
XM_017021982.1:c.242+1_242+2insC XP_016877471.1:n.242+1_242+2insC
XM_017021983.1:c.27-14993_27-14992insC XP_016877472.1:n.27-14993_27-14992insC
XM_017021984.1:c.992+1_992+2insC XP_016877473.1:n.992+1_992+2insC
XR_001751118.1:n.2875+1_2875+2insC
XR_001751119.1:n.2875+1_2875+2insC
XR_001751120.1:n.2875+1_2875+2insC
NM_139057.4:c.1721+1_1721+2insC MANE Select NP_620688.2:n.1721+1_1721+2insC