Canonical Allele Identifier: CA2199787145

Gene: ADAMTS17

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.99973200_99973203delinsCAAG , CM000677.2:g.99973200_99973203delinsCAAG	GRCh38
NC_000015.9:g.100513405_100513408delinsCAAG , CM000677.1:g.100513405_100513408delinsCAAG	GRCh37
NC_000015.8:g.98330928_98330931delinsCAAG	NCBI36
NG_016287.1:g.373776_373779delinsCTTG
NG_016287.2:g.373776_373779delinsCTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268070.9:c.*1199_*1202delinsCTTG MANE Select	ENSP00000268070.4:n.*1199_*1202delinsCTTG
ENST00000268070.8:c.*1199_*1202delinsCTTG	ENSP00000268070.4:n.*1199_*1202delinsCTTG
ENST00000557896.1:n.1498_1501delinsCTTG
NM_139057.2:c.*1199_*1202delinsCTTG	NP_620688.2:n.*1199_*1202delinsCTTG
XM_005254872.2:c.*1199_*1202delinsCTTG	XP_005254929.1:n.*1199_*1202delinsCTTG
XM_011521312.1:c.*1199_*1202delinsCTTG	XP_011519614.1:n.*1199_*1202delinsCTTG
XR_429624.2:n.1744-426_1744-423delinsCAAG
NM_139057.3:c.*1199_*1202delinsCTTG	NP_620688.2:n.*1199_*1202delinsCTTG
XM_005254872.3:c.*1199_*1202delinsCTTG	XP_005254929.1:n.*1199_*1202delinsCTTG
XM_011521312.2:c.*1199_*1202delinsCTTG	XP_011519614.1:n.*1199_*1202delinsCTTG
XM_017021973.2:c.*1199_*1202delinsCTTG	XP_016877462.1:n.*1199_*1202delinsCTTG
XM_017021975.1:c.*1199_*1202delinsCTTG	XP_016877464.1:n.*1199_*1202delinsCTTG
XM_017021976.1:c.*1199_*1202delinsCTTG	XP_016877465.1:n.*1199_*1202delinsCTTG
XM_017021978.1:c.*1199_*1202delinsCTTG	XP_016877467.1:n.*1199_*1202delinsCTTG
XM_017021979.1:c.*1199_*1202delinsCTTG	XP_016877468.1:n.*1199_*1202delinsCTTG
XM_017021980.1:c.*1199_*1202delinsCTTG	XP_016877469.1:n.*1199_*1202delinsCTTG
XM_017021982.1:c.*1199_*1202delinsCTTG	XP_016877471.1:n.*1199_*1202delinsCTTG
XM_017021983.1:c.*1199_*1202delinsCTTG	XP_016877472.1:n.*1199_*1202delinsCTTG
NM_139057.4:c.*1199_*1202delinsCTTG MANE Select	NP_620688.2:n.*1199_*1202delinsCTTG