Canonical Allele Identifier: CA393933487

Gene: ADAMTS17

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100132011G>T , CM000677.2:g.100132011G>T	GRCh38
NC_000015.9:g.100672216G>T , CM000677.1:g.100672216G>T	GRCh37
NC_000015.8:g.98489739G>T	NCBI36
NG_016287.1:g.214968C>A
NG_016287.2:g.214968C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268070.9:c.1717C>A MANE Select	ENSP00000268070.4:p.Pro573Thr
ENST00000568565.2:c.1717C>A	ENSP00000456161.2:p.Pro573Thr
ENST00000268070.8:c.1717C>A	ENSP00000268070.4:p.Pro573Thr
ENST00000378898.8:n.1398C>A
NM_139057.2:c.1717C>A	NP_620688.2:p.Pro573Thr
XM_005254872.2:c.1717C>A	XP_005254929.1:p.Pro573Thr
XM_011521312.1:c.1717C>A	XP_011519614.1:p.Pro573Thr
NM_139057.3:c.1717C>A	NP_620688.2:p.Pro573Thr
XM_005254872.3:c.1717C>A	XP_005254929.1:p.Pro573Thr
XM_011521312.2:c.1717C>A	XP_011519614.1:p.Pro573Thr
XM_017021973.2:c.1849C>A	XP_016877462.1:p.Pro617Thr
XM_017021974.1:c.1849C>A	XP_016877463.1:p.Pro617Thr
XM_017021975.1:c.1849C>A	XP_016877464.1:p.Pro617Thr
XM_017021976.1:c.1120C>A	XP_016877465.1:p.Pro374Thr
XM_017021977.1:c.1849C>A	XP_016877466.1:p.Pro617Thr
XM_017021978.1:c.751C>A	XP_016877467.1:p.Pro251Thr
XM_017021979.1:c.529C>A	XP_016877468.1:p.Pro177Thr
XM_017021980.1:c.529C>A	XP_016877469.1:p.Pro177Thr
XM_017021981.1:c.1849C>A	XP_016877470.1:p.Pro617Thr
XM_017021982.1:c.238C>A	XP_016877471.1:p.Pro80Thr
XM_017021983.1:c.27-14998C>A	XP_016877472.1:n.27-14998C>A
XM_017021984.1:c.988C>A	XP_016877473.1:p.Pro330Thr
XR_001751118.1:n.2871C>A
XR_001751119.1:n.2871C>A
XR_001751120.1:n.2871C>A
NM_139057.4:c.1717C>A MANE Select	NP_620688.2:p.Pro573Thr