Canonical Allele Identifier: CA2199864616

Gene: ADAMTS17

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100132111C= , CM000677.2:g.100132111C=	GRCh38
NC_000015.9:g.100672316C= , CM000677.1:g.100672316C=	GRCh37
NC_000015.8:g.98489839C=	NCBI36
NG_016287.1:g.214868G=
NG_016287.2:g.214868G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268070.9:c.1617G= MANE Select	ENSP00000268070.4:p.Pro539=
ENST00000568565.2:c.1617G=	ENSP00000456161.2:p.Pro539=
ENST00000268070.8:c.1617G=	ENSP00000268070.4:p.Pro539=
ENST00000378898.8:n.1298G=
NM_139057.2:c.1617G=	NP_620688.2:p.Pro539=
XM_005254872.2:c.1617G=	XP_005254929.1:p.Pro539=
XM_011521312.1:c.1617G=	XP_011519614.1:p.Pro539=
NM_139057.3:c.1617G=	NP_620688.2:p.Pro539=
XM_005254872.3:c.1617G=	XP_005254929.1:p.Pro539=
XM_011521312.2:c.1617G=	XP_011519614.1:p.Pro539=
XM_017021973.2:c.1749G=	XP_016877462.1:p.Pro583=
XM_017021974.1:c.1749G=	XP_016877463.1:p.Pro583=
XM_017021975.1:c.1749G=	XP_016877464.1:p.Pro583=
XM_017021976.1:c.1020G=	XP_016877465.1:p.Pro340=
XM_017021977.1:c.1749G=	XP_016877466.1:p.Pro583=
XM_017021978.1:c.651G=	XP_016877467.1:p.Pro217=
XM_017021979.1:c.429G=	XP_016877468.1:p.Pro143=
XM_017021980.1:c.429G=	XP_016877469.1:p.Pro143=
XM_017021981.1:c.1749G=	XP_016877470.1:p.Pro583=
XM_017021982.1:c.138G=	XP_016877471.1:p.Pro46=
XM_017021983.1:c.27-15098G=	XP_016877472.1:n.27-15098G=
XM_017021984.1:c.888G=	XP_016877473.1:p.Pro296=
XR_001751118.1:n.2771G=
XR_001751119.1:n.2771G=
XR_001751120.1:n.2771G=
NM_139057.4:c.1617G= MANE Select	NP_620688.2:p.Pro539=