Canonical Allele Identifier: CA2199964452

Gene: ADAMTS17

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100281304_100281305delinsCA , CM000677.2:g.100281304_100281305delinsCA	GRCh38
NC_000015.9:g.100821509_100821510delinsCA , CM000677.1:g.100821509_100821510delinsCA	GRCh37
NC_000015.8:g.98639032_98639033delinsCA	NCBI36
NG_016287.1:g.65674_65675delinsTG
NG_016287.2:g.65674_65675delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268070.9:c.713_714delinsTG MANE Select	ENSP00000268070.4:p.Val238=
ENST00000568565.2:c.713_714delinsTG	ENSP00000456161.2:p.Val238=
ENST00000268070.8:c.713_714delinsTG	ENSP00000268070.4:p.Val238=
ENST00000378898.8:n.394_395delinsTG
ENST00000558960.1:c.*135_*136delinsTG	ENSP00000453604.1:n.*135_*136delinsTG
NM_139057.2:c.713_714delinsTG	NP_620688.2:p.Val238=
XM_005254872.2:c.713_714delinsTG	XP_005254929.1:p.Val238=
XM_011521312.1:c.713_714delinsTG	XP_011519614.1:p.Val238=
NM_139057.3:c.713_714delinsTG	NP_620688.2:p.Val238=
XM_005254872.3:c.713_714delinsTG	XP_005254929.1:p.Val238=
XM_011521312.2:c.713_714delinsTG	XP_011519614.1:p.Val238=
XM_017021973.2:c.713_714delinsTG	XP_016877462.1:p.Val238=
XM_017021974.1:c.713_714delinsTG	XP_016877463.1:p.Val238=
XM_017021975.1:c.713_714delinsTG	XP_016877464.1:p.Val238=
XM_017021976.1:c.-17_-16delinsTG	XP_016877465.1:n.-17_-16delinsTG
XM_017021977.1:c.713_714delinsTG	XP_016877466.1:p.Val238=
XM_017021981.1:c.713_714delinsTG	XP_016877470.1:p.Val238=
XM_017021984.1:c.-17_-16delinsTG	XP_016877473.1:n.-17_-16delinsTG
XR_001751118.1:n.1735_1736delinsTG
XR_001751119.1:n.1735_1736delinsTG
XR_001751120.1:n.1735_1736delinsTG
NM_139057.4:c.713_714delinsTG MANE Select	NP_620688.2:p.Val238=