Canonical Allele Identifier: CA2630605987

Gene: ADAMTS17

Linked Data

• gnomAD v4: 15-100048738-CAAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100048741_100048743del , CM000677.2:g.100048741_100048743del	GRCh38
NC_000015.9:g.100588946_100588948del , CM000677.1:g.100588946_100588948del	GRCh37
NC_000015.8:g.98406469_98406471del	NCBI36
NG_016287.1:g.298238_298240del
NG_016287.2:g.298238_298240del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268070.9:c.2591+116_2591+118del MANE Select	ENSP00000268070.4:n.2591+116_2591+118del
ENST00000568565.2:c.2672+116_2672+118del	ENSP00000456161.2:n.2672+116_2672+118del
ENST00000268070.8:c.2591+116_2591+118del	ENSP00000268070.4:n.2591+116_2591+118del
NM_139057.2:c.2591+116_2591+118del	NP_620688.2:n.2591+116_2591+118del
XM_005254872.2:c.2672+116_2672+118del	XP_005254929.1:n.2672+116_2672+118del
XM_011521312.1:c.2741+116_2741+118del	XP_011519614.1:n.2741+116_2741+118del
NM_139057.3:c.2591+116_2591+118del	NP_620688.2:n.2591+116_2591+118del
XM_005254872.3:c.2672+116_2672+118del	XP_005254929.1:n.2672+116_2672+118del
XM_011521312.2:c.2741+116_2741+118del	XP_011519614.1:n.2741+116_2741+118del
XM_017021973.2:c.2873+116_2873+118del	XP_016877462.1:n.2873+116_2873+118del
XM_017021974.1:c.2873+116_2873+118del	XP_016877463.1:n.2873+116_2873+118del
XM_017021975.1:c.2804+116_2804+118del	XP_016877464.1:n.2804+116_2804+118del
XM_017021976.1:c.2144+116_2144+118del	XP_016877465.1:n.2144+116_2144+118del
XM_017021978.1:c.1775+116_1775+118del	XP_016877467.1:n.1775+116_1775+118del
XM_017021979.1:c.1553+116_1553+118del	XP_016877468.1:n.1553+116_1553+118del
XM_017021980.1:c.1553+116_1553+118del	XP_016877469.1:n.1553+116_1553+118del
XM_017021982.1:c.1262+116_1262+118del	XP_016877471.1:n.1262+116_1262+118del
XM_017021983.1:c.1046+116_1046+118del	XP_016877472.1:n.1046+116_1046+118del
NM_139057.4:c.2591+116_2591+118del MANE Select	NP_620688.2:n.2591+116_2591+118del