Canonical Allele Identifier: CA393692425
Gene: ADAMTS17 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.100048908C>T , CM000677.2:g.100048908C>T GRCh38
NC_000015.9:g.100589113C>T , CM000677.1:g.100589113C>T GRCh37
NC_000015.8:g.98406636C>T NCBI36
NG_016287.1:g.298071G>A
NG_016287.2:g.298071G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000268070.9:c.2540G>A MANE Select ENSP00000268070.4:p.Ser847Asn
ENST00000568565.2:c.2621G>A ENSP00000456161.2:p.Ser874Asn
ENST00000268070.8:c.2540G>A ENSP00000268070.4:p.Ser847Asn
NM_139057.2:c.2540G>A NP_620688.2:p.Ser847Asn
XM_005254872.2:c.2621G>A XP_005254929.1:p.Ser874Asn
XM_011521312.1:c.2690G>A XP_011519614.1:p.Ser897Asn
NM_139057.3:c.2540G>A NP_620688.2:p.Ser847Asn
XM_005254872.3:c.2621G>A XP_005254929.1:p.Ser874Asn
XM_011521312.2:c.2690G>A XP_011519614.1:p.Ser897Asn
XM_017021973.2:c.2822G>A XP_016877462.1:p.Ser941Asn
XM_017021974.1:c.2822G>A XP_016877463.1:p.Ser941Asn
XM_017021975.1:c.2753G>A XP_016877464.1:p.Ser918Asn
XM_017021976.1:c.2093G>A XP_016877465.1:p.Ser698Asn
XM_017021978.1:c.1724G>A XP_016877467.1:p.Ser575Asn
XM_017021979.1:c.1502G>A XP_016877468.1:p.Ser501Asn
XM_017021980.1:c.1502G>A XP_016877469.1:p.Ser501Asn
XM_017021982.1:c.1211G>A XP_016877471.1:p.Ser404Asn
XM_017021983.1:c.995G>A XP_016877472.1:p.Ser332Asn
NM_139057.4:c.2540G>A MANE Select NP_620688.2:p.Ser847Asn