Canonical Allele Identifier: CA393692382
Gene: ADAMTS17 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.100048899T>C , CM000677.2:g.100048899T>C GRCh38
NC_000015.9:g.100589104T>C , CM000677.1:g.100589104T>C GRCh37
NC_000015.8:g.98406627T>C NCBI36
NG_016287.1:g.298080A>G
NG_016287.2:g.298080A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000268070.9:c.2549A>G MANE Select ENSP00000268070.4:p.Glu850Gly
ENST00000568565.2:c.2630A>G ENSP00000456161.2:p.Glu877Gly
ENST00000268070.8:c.2549A>G ENSP00000268070.4:p.Glu850Gly
NM_139057.2:c.2549A>G NP_620688.2:p.Glu850Gly
XM_005254872.2:c.2630A>G XP_005254929.1:p.Glu877Gly
XM_011521312.1:c.2699A>G XP_011519614.1:p.Glu900Gly
NM_139057.3:c.2549A>G NP_620688.2:p.Glu850Gly
XM_005254872.3:c.2630A>G XP_005254929.1:p.Glu877Gly
XM_011521312.2:c.2699A>G XP_011519614.1:p.Glu900Gly
XM_017021973.2:c.2831A>G XP_016877462.1:p.Glu944Gly
XM_017021974.1:c.2831A>G XP_016877463.1:p.Glu944Gly
XM_017021975.1:c.2762A>G XP_016877464.1:p.Glu921Gly
XM_017021976.1:c.2102A>G XP_016877465.1:p.Glu701Gly
XM_017021978.1:c.1733A>G XP_016877467.1:p.Glu578Gly
XM_017021979.1:c.1511A>G XP_016877468.1:p.Glu504Gly
XM_017021980.1:c.1511A>G XP_016877469.1:p.Glu504Gly
XM_017021982.1:c.1220A>G XP_016877471.1:p.Glu407Gly
XM_017021983.1:c.1004A>G XP_016877472.1:p.Glu335Gly
NM_139057.4:c.2549A>G MANE Select NP_620688.2:p.Glu850Gly