Canonical Allele Identifier: CA2199964365
Gene: ADAMTS17 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.100281266T= , CM000677.2:g.100281266T= GRCh38
NC_000015.9:g.100821471T= , CM000677.1:g.100821471T= GRCh37
NC_000015.8:g.98638994T= NCBI36
NG_016287.1:g.65713A=
NG_016287.2:g.65713A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000268070.9:c.752A= MANE Select ENSP00000268070.4:p.Glu251=
ENST00000568565.2:c.752A= ENSP00000456161.2:p.Glu251=
ENST00000268070.8:c.752A= ENSP00000268070.4:p.Glu251=
ENST00000378898.8:n.433A=
ENST00000558960.1:c.*174A= ENSP00000453604.1:n.*174A=
NM_139057.2:c.752A= NP_620688.2:p.Glu251=
XM_005254872.2:c.752A= XP_005254929.1:p.Glu251=
XM_011521312.1:c.752A= XP_011519614.1:p.Glu251=
NM_139057.3:c.752A= NP_620688.2:p.Glu251=
XM_005254872.3:c.752A= XP_005254929.1:p.Glu251=
XM_011521312.2:c.752A= XP_011519614.1:p.Glu251=
XM_017021973.2:c.752A= XP_016877462.1:p.Glu251=
XM_017021974.1:c.752A= XP_016877463.1:p.Glu251=
XM_017021975.1:c.752A= XP_016877464.1:p.Glu251=
XM_017021976.1:c.23A= XP_016877465.1:p.Glu8=
XM_017021977.1:c.752A= XP_016877466.1:p.Glu251=
XM_017021981.1:c.752A= XP_016877470.1:p.Glu251=
XM_017021984.1:c.23A= XP_016877473.1:p.Glu8=
XR_001751118.1:n.1774A=
XR_001751119.1:n.1774A=
XR_001751120.1:n.1774A=
NM_139057.4:c.752A= MANE Select NP_620688.2:p.Glu251=