Canonical Allele Identifier: CA2199864604

Gene: ADAMTS17

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100132103A= , CM000677.2:g.100132103A=	GRCh38
NC_000015.9:g.100672308A= , CM000677.1:g.100672308A=	GRCh37
NC_000015.8:g.98489831A=	NCBI36
NG_016287.1:g.214876T=
NG_016287.2:g.214876T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268070.9:c.1625T= MANE Select	ENSP00000268070.4:p.Val542=
ENST00000568565.2:c.1625T=	ENSP00000456161.2:p.Val542=
ENST00000268070.8:c.1625T=	ENSP00000268070.4:p.Val542=
ENST00000378898.8:n.1306T=
NM_139057.2:c.1625T=	NP_620688.2:p.Val542=
XM_005254872.2:c.1625T=	XP_005254929.1:p.Val542=
XM_011521312.1:c.1625T=	XP_011519614.1:p.Val542=
NM_139057.3:c.1625T=	NP_620688.2:p.Val542=
XM_005254872.3:c.1625T=	XP_005254929.1:p.Val542=
XM_011521312.2:c.1625T=	XP_011519614.1:p.Val542=
XM_017021973.2:c.1757T=	XP_016877462.1:p.Val586=
XM_017021974.1:c.1757T=	XP_016877463.1:p.Val586=
XM_017021975.1:c.1757T=	XP_016877464.1:p.Val586=
XM_017021976.1:c.1028T=	XP_016877465.1:p.Val343=
XM_017021977.1:c.1757T=	XP_016877466.1:p.Val586=
XM_017021978.1:c.659T=	XP_016877467.1:p.Val220=
XM_017021979.1:c.437T=	XP_016877468.1:p.Val146=
XM_017021980.1:c.437T=	XP_016877469.1:p.Val146=
XM_017021981.1:c.1757T=	XP_016877470.1:p.Val586=
XM_017021982.1:c.146T=	XP_016877471.1:p.Val49=
XM_017021983.1:c.27-15090T=	XP_016877472.1:n.27-15090T=
XM_017021984.1:c.896T=	XP_016877473.1:p.Val299=
XR_001751118.1:n.2779T=
XR_001751119.1:n.2779T=
XR_001751120.1:n.2779T=
NM_139057.4:c.1625T= MANE Select	NP_620688.2:p.Val542=