Canonical Allele Identifier: CA717852872

Gene: ADAMTS17

Linked Data

• dbSNP Id: rs1432758061
• MyVariant Identifiers: chr15:g.100513302_100513304del (hg19) ; chr15:g.99973097_99973099del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.99973099_99973101del , CM000677.2:g.99973099_99973101del	GRCh38
NC_000015.9:g.100513304_100513306del , CM000677.1:g.100513304_100513306del	GRCh37
NC_000015.8:g.98330827_98330829del	NCBI36
NG_016287.1:g.373880_373882del
NG_016287.2:g.373880_373882del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268070.9:c.*1303_*1305del MANE Select	ENSP00000268070.4:n.*1303_*1305del
ENST00000268070.8:c.*1303_*1305del	ENSP00000268070.4:n.*1303_*1305del
ENST00000557896.1:n.1602_1604del
NM_139057.2:c.*1303_*1305del	NP_620688.2:n.*1303_*1305del
XM_005254872.2:c.*1303_*1305del	XP_005254929.1:n.*1303_*1305del
XM_011521312.1:c.*1303_*1305del	XP_011519614.1:n.*1303_*1305del
XR_429624.2:n.1743+366_1743+368del
NM_139057.3:c.*1303_*1305del	NP_620688.2:n.*1303_*1305del
XM_005254872.3:c.*1303_*1305del	XP_005254929.1:n.*1303_*1305del
XM_011521312.2:c.*1303_*1305del	XP_011519614.1:n.*1303_*1305del
XM_017021973.2:c.*1303_*1305del	XP_016877462.1:n.*1303_*1305del
XM_017021975.1:c.*1303_*1305del	XP_016877464.1:n.*1303_*1305del
XM_017021976.1:c.*1303_*1305del	XP_016877465.1:n.*1303_*1305del
XM_017021978.1:c.*1303_*1305del	XP_016877467.1:n.*1303_*1305del
XM_017021979.1:c.*1303_*1305del	XP_016877468.1:n.*1303_*1305del
XM_017021980.1:c.*1303_*1305del	XP_016877469.1:n.*1303_*1305del
XM_017021982.1:c.*1303_*1305del	XP_016877471.1:n.*1303_*1305del
XM_017021983.1:c.*1303_*1305del	XP_016877472.1:n.*1303_*1305del
NM_139057.4:c.*1303_*1305del MANE Select	NP_620688.2:n.*1303_*1305del