Canonical Allele Identifier: CA2199864596

Gene: ADAMTS17

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100132098C= , CM000677.2:g.100132098C=	GRCh38
NC_000015.9:g.100672303C= , CM000677.1:g.100672303C=	GRCh37
NC_000015.8:g.98489826C=	NCBI36
NG_016287.1:g.214881G=
NG_016287.2:g.214881G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268070.9:c.1630G= MANE Select	ENSP00000268070.4:p.Gly544=
ENST00000568565.2:c.1630G=	ENSP00000456161.2:p.Gly544=
ENST00000268070.8:c.1630G=	ENSP00000268070.4:p.Gly544=
ENST00000378898.8:n.1311G=
NM_139057.2:c.1630G=	NP_620688.2:p.Gly544=
XM_005254872.2:c.1630G=	XP_005254929.1:p.Gly544=
XM_011521312.1:c.1630G=	XP_011519614.1:p.Gly544=
NM_139057.3:c.1630G=	NP_620688.2:p.Gly544=
XM_005254872.3:c.1630G=	XP_005254929.1:p.Gly544=
XM_011521312.2:c.1630G=	XP_011519614.1:p.Gly544=
XM_017021973.2:c.1762G=	XP_016877462.1:p.Gly588=
XM_017021974.1:c.1762G=	XP_016877463.1:p.Gly588=
XM_017021975.1:c.1762G=	XP_016877464.1:p.Gly588=
XM_017021976.1:c.1033G=	XP_016877465.1:p.Gly345=
XM_017021977.1:c.1762G=	XP_016877466.1:p.Gly588=
XM_017021978.1:c.664G=	XP_016877467.1:p.Gly222=
XM_017021979.1:c.442G=	XP_016877468.1:p.Gly148=
XM_017021980.1:c.442G=	XP_016877469.1:p.Gly148=
XM_017021981.1:c.1762G=	XP_016877470.1:p.Gly588=
XM_017021982.1:c.151G=	XP_016877471.1:p.Gly51=
XM_017021983.1:c.27-15085G=	XP_016877472.1:n.27-15085G=
XM_017021984.1:c.901G=	XP_016877473.1:p.Gly301=
XR_001751118.1:n.2784G=
XR_001751119.1:n.2784G=
XR_001751120.1:n.2784G=
NM_139057.4:c.1630G= MANE Select	NP_620688.2:p.Gly544=