Canonical Allele Identifier: CA2199825577

Gene: ADAMTS17

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100048900C= , CM000677.2:g.100048900C=	GRCh38
NC_000015.9:g.100589105C= , CM000677.1:g.100589105C=	GRCh37
NC_000015.8:g.98406628C=	NCBI36
NG_016287.1:g.298079G=
NG_016287.2:g.298079G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268070.9:c.2548G= MANE Select	ENSP00000268070.4:p.Glu850=
ENST00000568565.2:c.2629G=	ENSP00000456161.2:p.Glu877=
ENST00000268070.8:c.2548G=	ENSP00000268070.4:p.Glu850=
NM_139057.2:c.2548G=	NP_620688.2:p.Glu850=
XM_005254872.2:c.2629G=	XP_005254929.1:p.Glu877=
XM_011521312.1:c.2698G=	XP_011519614.1:p.Glu900=
NM_139057.3:c.2548G=	NP_620688.2:p.Glu850=
XM_005254872.3:c.2629G=	XP_005254929.1:p.Glu877=
XM_011521312.2:c.2698G=	XP_011519614.1:p.Glu900=
XM_017021973.2:c.2830G=	XP_016877462.1:p.Glu944=
XM_017021974.1:c.2830G=	XP_016877463.1:p.Glu944=
XM_017021975.1:c.2761G=	XP_016877464.1:p.Glu921=
XM_017021976.1:c.2101G=	XP_016877465.1:p.Glu701=
XM_017021978.1:c.1732G=	XP_016877467.1:p.Glu578=
XM_017021979.1:c.1510G=	XP_016877468.1:p.Glu504=
XM_017021980.1:c.1510G=	XP_016877469.1:p.Glu504=
XM_017021982.1:c.1219G=	XP_016877471.1:p.Glu407=
XM_017021983.1:c.1003G=	XP_016877472.1:p.Glu335=
NM_139057.4:c.2548G= MANE Select	NP_620688.2:p.Glu850=