Canonical Allele Identifier: CA2199825468

Gene: ADAMTS17

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100048688C= , CM000677.2:g.100048688C=	GRCh38
NC_000015.9:g.100588893C= , CM000677.1:g.100588893C=	GRCh37
NC_000015.8:g.98406416C=	NCBI36
NG_016287.1:g.298291G=
NG_016287.2:g.298291G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268070.9:c.2591+169G= MANE Select	ENSP00000268070.4:n.2591+169G=
ENST00000568565.2:c.2672+169G=	ENSP00000456161.2:n.2672+169G=
ENST00000268070.8:c.2591+169G=	ENSP00000268070.4:n.2591+169G=
NM_139057.2:c.2591+169G=	NP_620688.2:n.2591+169G=
XM_005254872.2:c.2672+169G=	XP_005254929.1:n.2672+169G=
XM_011521312.1:c.2741+169G=	XP_011519614.1:n.2741+169G=
NM_139057.3:c.2591+169G=	NP_620688.2:n.2591+169G=
XM_005254872.3:c.2672+169G=	XP_005254929.1:n.2672+169G=
XM_011521312.2:c.2741+169G=	XP_011519614.1:n.2741+169G=
XM_017021973.2:c.2873+169G=	XP_016877462.1:n.2873+169G=
XM_017021974.1:c.2873+169G=	XP_016877463.1:n.2873+169G=
XM_017021975.1:c.2804+169G=	XP_016877464.1:n.2804+169G=
XM_017021976.1:c.2144+169G=	XP_016877465.1:n.2144+169G=
XM_017021978.1:c.1775+169G=	XP_016877467.1:n.1775+169G=
XM_017021979.1:c.1553+169G=	XP_016877468.1:n.1553+169G=
XM_017021980.1:c.1553+169G=	XP_016877469.1:n.1553+169G=
XM_017021982.1:c.1262+169G=	XP_016877471.1:n.1262+169G=
XM_017021983.1:c.1046+169G=	XP_016877472.1:n.1046+169G=
NM_139057.4:c.2591+169G= MANE Select	NP_620688.2:n.2591+169G=