Canonical Allele Identifier: CA2199964562

Gene: ADAMTS17

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100281351T= , CM000677.2:g.100281351T=	GRCh38
NC_000015.9:g.100821556T= , CM000677.1:g.100821556T=	GRCh37
NC_000015.8:g.98639079T=	NCBI36
NG_016287.1:g.65628A=
NG_016287.2:g.65628A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268070.9:c.667A= MANE Select	ENSP00000268070.4:p.Arg223=
ENST00000568565.2:c.667A=	ENSP00000456161.2:p.Arg223=
ENST00000268070.8:c.667A=	ENSP00000268070.4:p.Arg223=
ENST00000378898.8:n.348A=
ENST00000558960.1:c.*89A=	ENSP00000453604.1:n.*89A=
NM_139057.2:c.667A=	NP_620688.2:p.Arg223=
XM_005254872.2:c.667A=	XP_005254929.1:p.Arg223=
XM_011521312.1:c.667A=	XP_011519614.1:p.Arg223=
NM_139057.3:c.667A=	NP_620688.2:p.Arg223=
XM_005254872.3:c.667A=	XP_005254929.1:p.Arg223=
XM_011521312.2:c.667A=	XP_011519614.1:p.Arg223=
XM_017021973.2:c.667A=	XP_016877462.1:p.Arg223=
XM_017021974.1:c.667A=	XP_016877463.1:p.Arg223=
XM_017021975.1:c.667A=	XP_016877464.1:p.Arg223=
XM_017021976.1:c.-63A=	XP_016877465.1:n.-63A=
XM_017021977.1:c.667A=	XP_016877466.1:p.Arg223=
XM_017021981.1:c.667A=	XP_016877470.1:p.Arg223=
XM_017021984.1:c.-63A=	XP_016877473.1:n.-63A=
XR_001751118.1:n.1689A=
XR_001751119.1:n.1689A=
XR_001751120.1:n.1689A=
NM_139057.4:c.667A= MANE Select	NP_620688.2:p.Arg223=