Canonical Allele Identifier: CA393692417
Gene: ADAMTS17 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.100048907G>C , CM000677.2:g.100048907G>C GRCh38
NC_000015.9:g.100589112G>C , CM000677.1:g.100589112G>C GRCh37
NC_000015.8:g.98406635G>C NCBI36
NG_016287.1:g.298072C>G
NG_016287.2:g.298072C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000268070.9:c.2541C>G MANE Select ENSP00000268070.4:p.Ser847Arg
ENST00000568565.2:c.2622C>G ENSP00000456161.2:p.Ser874Arg
ENST00000268070.8:c.2541C>G ENSP00000268070.4:p.Ser847Arg
NM_139057.2:c.2541C>G NP_620688.2:p.Ser847Arg
XM_005254872.2:c.2622C>G XP_005254929.1:p.Ser874Arg
XM_011521312.1:c.2691C>G XP_011519614.1:p.Ser897Arg
NM_139057.3:c.2541C>G NP_620688.2:p.Ser847Arg
XM_005254872.3:c.2622C>G XP_005254929.1:p.Ser874Arg
XM_011521312.2:c.2691C>G XP_011519614.1:p.Ser897Arg
XM_017021973.2:c.2823C>G XP_016877462.1:p.Ser941Arg
XM_017021974.1:c.2823C>G XP_016877463.1:p.Ser941Arg
XM_017021975.1:c.2754C>G XP_016877464.1:p.Ser918Arg
XM_017021976.1:c.2094C>G XP_016877465.1:p.Ser698Arg
XM_017021978.1:c.1725C>G XP_016877467.1:p.Ser575Arg
XM_017021979.1:c.1503C>G XP_016877468.1:p.Ser501Arg
XM_017021980.1:c.1503C>G XP_016877469.1:p.Ser501Arg
XM_017021982.1:c.1212C>G XP_016877471.1:p.Ser404Arg
XM_017021983.1:c.996C>G XP_016877472.1:p.Ser332Arg
NM_139057.4:c.2541C>G MANE Select NP_620688.2:p.Ser847Arg