Canonical Allele Identifier: CA492369933

Gene: ADAMTS17

Linked Data

• MyVariant Identifiers: chr15:g.100589103C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100048898C>T , CM000677.2:g.100048898C>T	GRCh38
NC_000015.9:g.100589103C>T , CM000677.1:g.100589103C>T	GRCh37
NC_000015.8:g.98406626C>T	NCBI36
NG_016287.1:g.298081G>A
NG_016287.2:g.298081G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268070.9:c.2550G>A MANE Select	ENSP00000268070.4:p.Glu850=
ENST00000568565.2:c.2631G>A	ENSP00000456161.2:p.Glu877=
ENST00000268070.8:c.2550G>A	ENSP00000268070.4:p.Glu850=
NM_139057.2:c.2550G>A	NP_620688.2:p.Glu850=
XM_005254872.2:c.2631G>A	XP_005254929.1:p.Glu877=
XM_011521312.1:c.2700G>A	XP_011519614.1:p.Glu900=
NM_139057.3:c.2550G>A	NP_620688.2:p.Glu850=
XM_005254872.3:c.2631G>A	XP_005254929.1:p.Glu877=
XM_011521312.2:c.2700G>A	XP_011519614.1:p.Glu900=
XM_017021973.2:c.2832G>A	XP_016877462.1:p.Glu944=
XM_017021974.1:c.2832G>A	XP_016877463.1:p.Glu944=
XM_017021975.1:c.2763G>A	XP_016877464.1:p.Glu921=
XM_017021976.1:c.2103G>A	XP_016877465.1:p.Glu701=
XM_017021978.1:c.1734G>A	XP_016877467.1:p.Glu578=
XM_017021979.1:c.1512G>A	XP_016877468.1:p.Glu504=
XM_017021980.1:c.1512G>A	XP_016877469.1:p.Glu504=
XM_017021982.1:c.1221G>A	XP_016877471.1:p.Glu407=
XM_017021983.1:c.1005G>A	XP_016877472.1:p.Glu335=
NM_139057.4:c.2550G>A MANE Select	NP_620688.2:p.Glu850=