Canonical Allele Identifier: CA2199864454

Gene: ADAMTS17

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100132008G= , CM000677.2:g.100132008G=	GRCh38
NC_000015.9:g.100672213G= , CM000677.1:g.100672213G=	GRCh37
NC_000015.8:g.98489736G=	NCBI36
NG_016287.1:g.214971C=
NG_016287.2:g.214971C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268070.9:c.1720C= MANE Select	ENSP00000268070.4:p.Pro574=
ENST00000568565.2:c.1720C=	ENSP00000456161.2:p.Pro574=
ENST00000268070.8:c.1720C=	ENSP00000268070.4:p.Pro574=
ENST00000378898.8:n.1401C=
NM_139057.2:c.1720C=	NP_620688.2:p.Pro574=
XM_005254872.2:c.1720C=	XP_005254929.1:p.Pro574=
XM_011521312.1:c.1720C=	XP_011519614.1:p.Pro574=
NM_139057.3:c.1720C=	NP_620688.2:p.Pro574=
XM_005254872.3:c.1720C=	XP_005254929.1:p.Pro574=
XM_011521312.2:c.1720C=	XP_011519614.1:p.Pro574=
XM_017021973.2:c.1852C=	XP_016877462.1:p.Pro618=
XM_017021974.1:c.1852C=	XP_016877463.1:p.Pro618=
XM_017021975.1:c.1852C=	XP_016877464.1:p.Pro618=
XM_017021976.1:c.1123C=	XP_016877465.1:p.Pro375=
XM_017021977.1:c.1852C=	XP_016877466.1:p.Pro618=
XM_017021978.1:c.754C=	XP_016877467.1:p.Pro252=
XM_017021979.1:c.532C=	XP_016877468.1:p.Pro178=
XM_017021980.1:c.532C=	XP_016877469.1:p.Pro178=
XM_017021981.1:c.1852C=	XP_016877470.1:p.Pro618=
XM_017021982.1:c.241C=	XP_016877471.1:p.Pro81=
XM_017021983.1:c.27-14995C=	XP_016877472.1:n.27-14995C=
XM_017021984.1:c.991C=	XP_016877473.1:p.Pro331=
XR_001751118.1:n.2874C=
XR_001751119.1:n.2874C=
XR_001751120.1:n.2874C=
NM_139057.4:c.1720C= MANE Select	NP_620688.2:p.Pro574=