Canonical Allele Identifier: CA2199998030

Gene: ADAMTS17

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100341322G= , CM000677.2:g.100341322G=	GRCh38
NC_000015.9:g.100881527G= , CM000677.1:g.100881527G=	GRCh37
NC_000015.8:g.98699050G=	NCBI36
NG_016287.1:g.5657C=
NG_016287.2:g.5657C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000268070.9:c.167C= MANE Select	ENSP00000268070.4:p.Ala56=
ENST00000568565.2:c.167C=	ENSP00000456161.2:p.Ala56=
ENST00000268070.8:c.167C=	ENSP00000268070.4:p.Ala56=
ENST00000558960.1:c.79+499C=	ENSP00000453604.1:n.79+499C=
NM_139057.2:c.167C=	NP_620688.2:p.Ala56=
XM_005254872.2:c.167C=	XP_005254929.1:p.Ala56=
XM_011521312.1:c.167C=	XP_011519614.1:p.Ala56=
NM_139057.3:c.167C=	NP_620688.2:p.Ala56=
XM_005254872.3:c.167C=	XP_005254929.1:p.Ala56=
XM_011521312.2:c.167C=	XP_011519614.1:p.Ala56=
XM_017021973.2:c.167C=	XP_016877462.1:p.Ala56=
XM_017021974.1:c.167C=	XP_016877463.1:p.Ala56=
XM_017021975.1:c.167C=	XP_016877464.1:p.Ala56=
XM_017021976.1:c.-280+499C=	XP_016877465.1:n.-280+499C=
XM_017021977.1:c.167C=	XP_016877466.1:p.Ala56=
XM_017021981.1:c.167C=	XP_016877470.1:p.Ala56=
XR_001751118.1:n.1189C=
XR_001751119.1:n.1189C=
XR_001751120.1:n.1189C=
NM_139057.4:c.167C= MANE Select	NP_620688.2:p.Ala56=