Canonical Allele Identifier: CA2199825580

Gene: ADAMTS17

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100048906G= , CM000677.2:g.100048906G=	GRCh38
NC_000015.9:g.100589111G= , CM000677.1:g.100589111G=	GRCh37
NC_000015.8:g.98406634G=	NCBI36
NG_016287.1:g.298073C=
NG_016287.2:g.298073C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268070.9:c.2542C= MANE Select	ENSP00000268070.4:p.Arg848=
ENST00000568565.2:c.2623C=	ENSP00000456161.2:p.Arg875=
ENST00000268070.8:c.2542C=	ENSP00000268070.4:p.Arg848=
NM_139057.2:c.2542C=	NP_620688.2:p.Arg848=
XM_005254872.2:c.2623C=	XP_005254929.1:p.Arg875=
XM_011521312.1:c.2692C=	XP_011519614.1:p.Arg898=
NM_139057.3:c.2542C=	NP_620688.2:p.Arg848=
XM_005254872.3:c.2623C=	XP_005254929.1:p.Arg875=
XM_011521312.2:c.2692C=	XP_011519614.1:p.Arg898=
XM_017021973.2:c.2824C=	XP_016877462.1:p.Arg942=
XM_017021974.1:c.2824C=	XP_016877463.1:p.Arg942=
XM_017021975.1:c.2755C=	XP_016877464.1:p.Arg919=
XM_017021976.1:c.2095C=	XP_016877465.1:p.Arg699=
XM_017021978.1:c.1726C=	XP_016877467.1:p.Arg576=
XM_017021979.1:c.1504C=	XP_016877468.1:p.Arg502=
XM_017021980.1:c.1504C=	XP_016877469.1:p.Arg502=
XM_017021982.1:c.1213C=	XP_016877471.1:p.Arg405=
XM_017021983.1:c.997C=	XP_016877472.1:p.Arg333=
NM_139057.4:c.2542C= MANE Select	NP_620688.2:p.Arg848=