Canonical Allele Identifier: CA2199864609

Gene: ADAMTS17

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100132106T= , CM000677.2:g.100132106T=	GRCh38
NC_000015.9:g.100672311T= , CM000677.1:g.100672311T=	GRCh37
NC_000015.8:g.98489834T=	NCBI36
NG_016287.1:g.214873A=
NG_016287.2:g.214873A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268070.9:c.1622A= MANE Select	ENSP00000268070.4:p.His541=
ENST00000568565.2:c.1622A=	ENSP00000456161.2:p.His541=
ENST00000268070.8:c.1622A=	ENSP00000268070.4:p.His541=
ENST00000378898.8:n.1303A=
NM_139057.2:c.1622A=	NP_620688.2:p.His541=
XM_005254872.2:c.1622A=	XP_005254929.1:p.His541=
XM_011521312.1:c.1622A=	XP_011519614.1:p.His541=
NM_139057.3:c.1622A=	NP_620688.2:p.His541=
XM_005254872.3:c.1622A=	XP_005254929.1:p.His541=
XM_011521312.2:c.1622A=	XP_011519614.1:p.His541=
XM_017021973.2:c.1754A=	XP_016877462.1:p.His585=
XM_017021974.1:c.1754A=	XP_016877463.1:p.His585=
XM_017021975.1:c.1754A=	XP_016877464.1:p.His585=
XM_017021976.1:c.1025A=	XP_016877465.1:p.His342=
XM_017021977.1:c.1754A=	XP_016877466.1:p.His585=
XM_017021978.1:c.656A=	XP_016877467.1:p.His219=
XM_017021979.1:c.434A=	XP_016877468.1:p.His145=
XM_017021980.1:c.434A=	XP_016877469.1:p.His145=
XM_017021981.1:c.1754A=	XP_016877470.1:p.His585=
XM_017021982.1:c.143A=	XP_016877471.1:p.His48=
XM_017021983.1:c.27-15093A=	XP_016877472.1:n.27-15093A=
XM_017021984.1:c.893A=	XP_016877473.1:p.His298=
XR_001751118.1:n.2776A=
XR_001751119.1:n.2776A=
XR_001751120.1:n.2776A=
NM_139057.4:c.1622A= MANE Select	NP_620688.2:p.His541=