Canonical Allele Identifier: CA2199964545

Gene: ADAMTS17

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100281346G= , CM000677.2:g.100281346G=	GRCh38
NC_000015.9:g.100821551G= , CM000677.1:g.100821551G=	GRCh37
NC_000015.8:g.98639074G=	NCBI36
NG_016287.1:g.65633C=
NG_016287.2:g.65633C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268070.9:c.672C= MANE Select	ENSP00000268070.4:p.Asn224=
ENST00000568565.2:c.672C=	ENSP00000456161.2:p.Asn224=
ENST00000268070.8:c.672C=	ENSP00000268070.4:p.Asn224=
ENST00000378898.8:n.353C=
ENST00000558960.1:c.*94C=	ENSP00000453604.1:n.*94C=
NM_139057.2:c.672C=	NP_620688.2:p.Asn224=
XM_005254872.2:c.672C=	XP_005254929.1:p.Asn224=
XM_011521312.1:c.672C=	XP_011519614.1:p.Asn224=
NM_139057.3:c.672C=	NP_620688.2:p.Asn224=
XM_005254872.3:c.672C=	XP_005254929.1:p.Asn224=
XM_011521312.2:c.672C=	XP_011519614.1:p.Asn224=
XM_017021973.2:c.672C=	XP_016877462.1:p.Asn224=
XM_017021974.1:c.672C=	XP_016877463.1:p.Asn224=
XM_017021975.1:c.672C=	XP_016877464.1:p.Asn224=
XM_017021976.1:c.-58C=	XP_016877465.1:n.-58C=
XM_017021977.1:c.672C=	XP_016877466.1:p.Asn224=
XM_017021981.1:c.672C=	XP_016877470.1:p.Asn224=
XM_017021984.1:c.-58C=	XP_016877473.1:n.-58C=
XR_001751118.1:n.1694C=
XR_001751119.1:n.1694C=
XR_001751120.1:n.1694C=
NM_139057.4:c.672C= MANE Select	NP_620688.2:p.Asn224=