Canonical Allele Identifier: CA2805445418

Gene: ADAMTS17

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100048719del , CM000677.2:g.100048719del	GRCh38
NC_000015.9:g.100588924del , CM000677.1:g.100588924del	GRCh37
NC_000015.8:g.98406447del	NCBI36
NG_016287.1:g.298261del
NG_016287.2:g.298261del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268070.9:c.2591+139del MANE Select	ENSP00000268070.4:n.2591+139del
ENST00000568565.2:c.2672+139del	ENSP00000456161.2:n.2672+139del
ENST00000268070.8:c.2591+139del	ENSP00000268070.4:n.2591+139del
NM_139057.2:c.2591+139del	NP_620688.2:n.2591+139del
XM_005254872.2:c.2672+139del	XP_005254929.1:n.2672+139del
XM_011521312.1:c.2741+139del	XP_011519614.1:n.2741+139del
NM_139057.3:c.2591+139del	NP_620688.2:n.2591+139del
XM_005254872.3:c.2672+139del	XP_005254929.1:n.2672+139del
XM_011521312.2:c.2741+139del	XP_011519614.1:n.2741+139del
XM_017021973.2:c.2873+139del	XP_016877462.1:n.2873+139del
XM_017021974.1:c.2873+139del	XP_016877463.1:n.2873+139del
XM_017021975.1:c.2804+139del	XP_016877464.1:n.2804+139del
XM_017021976.1:c.2144+139del	XP_016877465.1:n.2144+139del
XM_017021978.1:c.1775+139del	XP_016877467.1:n.1775+139del
XM_017021979.1:c.1553+139del	XP_016877468.1:n.1553+139del
XM_017021980.1:c.1553+139del	XP_016877469.1:n.1553+139del
XM_017021982.1:c.1262+139del	XP_016877471.1:n.1262+139del
XM_017021983.1:c.1046+139del	XP_016877472.1:n.1046+139del
NM_139057.4:c.2591+139del MANE Select	NP_620688.2:n.2591+139del