Canonical Allele Identifier: CA393692421
Gene: ADAMTS17 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000268070.9:c.2540G>T MANE Select ENSP00000268070.4:p.Ser847Ile
ENST00000568565.2:c.2621G>T ENSP00000456161.2:p.Ser874Ile
ENST00000268070.8:c.2540G>T ENSP00000268070.4:p.Ser847Ile
NM_139057.2:c.2540G>T NP_620688.2:p.Ser847Ile
XM_005254872.2:c.2621G>T XP_005254929.1:p.Ser874Ile
XM_011521312.1:c.2690G>T XP_011519614.1:p.Ser897Ile
NM_139057.3:c.2540G>T NP_620688.2:p.Ser847Ile
XM_005254872.3:c.2621G>T XP_005254929.1:p.Ser874Ile
XM_011521312.2:c.2690G>T XP_011519614.1:p.Ser897Ile
XM_017021973.2:c.2822G>T XP_016877462.1:p.Ser941Ile
XM_017021974.1:c.2822G>T XP_016877463.1:p.Ser941Ile
XM_017021975.1:c.2753G>T XP_016877464.1:p.Ser918Ile
XM_017021976.1:c.2093G>T XP_016877465.1:p.Ser698Ile
XM_017021978.1:c.1724G>T XP_016877467.1:p.Ser575Ile
XM_017021979.1:c.1502G>T XP_016877468.1:p.Ser501Ile
XM_017021980.1:c.1502G>T XP_016877469.1:p.Ser501Ile
XM_017021982.1:c.1211G>T XP_016877471.1:p.Ser404Ile
XM_017021983.1:c.995G>T XP_016877472.1:p.Ser332Ile
NM_139057.4:c.2540G>T MANE Select NP_620688.2:p.Ser847Ile