Canonical Allele Identifier: CA919631683

Gene: ADAMTS17

Linked Data

• dbSNP Id: rs1596300191

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100048734_100048736del , CM000677.2:g.100048734_100048736del	GRCh38
NC_000015.9:g.100588939_100588941del , CM000677.1:g.100588939_100588941del	GRCh37
NC_000015.8:g.98406462_98406464del	NCBI36
NG_016287.1:g.298246_298248del
NG_016287.2:g.298246_298248del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268070.9:c.2591+124_2591+126del MANE Select	ENSP00000268070.4:n.2591+124_2591+126del
ENST00000568565.2:c.2672+124_2672+126del	ENSP00000456161.2:n.2672+124_2672+126del
ENST00000268070.8:c.2591+124_2591+126del	ENSP00000268070.4:n.2591+124_2591+126del
NM_139057.2:c.2591+124_2591+126del	NP_620688.2:n.2591+124_2591+126del
XM_005254872.2:c.2672+124_2672+126del	XP_005254929.1:n.2672+124_2672+126del
XM_011521312.1:c.2741+124_2741+126del	XP_011519614.1:n.2741+124_2741+126del
NM_139057.3:c.2591+124_2591+126del	NP_620688.2:n.2591+124_2591+126del
XM_005254872.3:c.2672+124_2672+126del	XP_005254929.1:n.2672+124_2672+126del
XM_011521312.2:c.2741+124_2741+126del	XP_011519614.1:n.2741+124_2741+126del
XM_017021973.2:c.2873+124_2873+126del	XP_016877462.1:n.2873+124_2873+126del
XM_017021974.1:c.2873+124_2873+126del	XP_016877463.1:n.2873+124_2873+126del
XM_017021975.1:c.2804+124_2804+126del	XP_016877464.1:n.2804+124_2804+126del
XM_017021976.1:c.2144+124_2144+126del	XP_016877465.1:n.2144+124_2144+126del
XM_017021978.1:c.1775+124_1775+126del	XP_016877467.1:n.1775+124_1775+126del
XM_017021979.1:c.1553+124_1553+126del	XP_016877468.1:n.1553+124_1553+126del
XM_017021980.1:c.1553+124_1553+126del	XP_016877469.1:n.1553+124_1553+126del
XM_017021982.1:c.1262+124_1262+126del	XP_016877471.1:n.1262+124_1262+126del
XM_017021983.1:c.1046+124_1046+126del	XP_016877472.1:n.1046+124_1046+126del
NM_139057.4:c.2591+124_2591+126del MANE Select	NP_620688.2:n.2591+124_2591+126del