Canonical Allele Identifier: CA2630606019

Gene: ADAMTS17

Linked Data

• gnomAD v4: 15-100048776-AACT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100048777_100048779del , CM000677.2:g.100048777_100048779del	GRCh38
NC_000015.9:g.100588982_100588984del , CM000677.1:g.100588982_100588984del	GRCh37
NC_000015.8:g.98406505_98406507del	NCBI36
NG_016287.1:g.298200_298202del
NG_016287.2:g.298200_298202del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268070.9:c.2591+78_2591+80del MANE Select	ENSP00000268070.4:n.2591+78_2591+80del
ENST00000568565.2:c.2672+78_2672+80del	ENSP00000456161.2:n.2672+78_2672+80del
ENST00000268070.8:c.2591+78_2591+80del	ENSP00000268070.4:n.2591+78_2591+80del
NM_139057.2:c.2591+78_2591+80del	NP_620688.2:n.2591+78_2591+80del
XM_005254872.2:c.2672+78_2672+80del	XP_005254929.1:n.2672+78_2672+80del
XM_011521312.1:c.2741+78_2741+80del	XP_011519614.1:n.2741+78_2741+80del
NM_139057.3:c.2591+78_2591+80del	NP_620688.2:n.2591+78_2591+80del
XM_005254872.3:c.2672+78_2672+80del	XP_005254929.1:n.2672+78_2672+80del
XM_011521312.2:c.2741+78_2741+80del	XP_011519614.1:n.2741+78_2741+80del
XM_017021973.2:c.2873+78_2873+80del	XP_016877462.1:n.2873+78_2873+80del
XM_017021974.1:c.2873+78_2873+80del	XP_016877463.1:n.2873+78_2873+80del
XM_017021975.1:c.2804+78_2804+80del	XP_016877464.1:n.2804+78_2804+80del
XM_017021976.1:c.2144+78_2144+80del	XP_016877465.1:n.2144+78_2144+80del
XM_017021978.1:c.1775+78_1775+80del	XP_016877467.1:n.1775+78_1775+80del
XM_017021979.1:c.1553+78_1553+80del	XP_016877468.1:n.1553+78_1553+80del
XM_017021980.1:c.1553+78_1553+80del	XP_016877469.1:n.1553+78_1553+80del
XM_017021982.1:c.1262+78_1262+80del	XP_016877471.1:n.1262+78_1262+80del
XM_017021983.1:c.1046+78_1046+80del	XP_016877472.1:n.1046+78_1046+80del
NM_139057.4:c.2591+78_2591+80del MANE Select	NP_620688.2:n.2591+78_2591+80del