Canonical Allele Identifier: CA4168511
Community Standard Title: NM_001004320.2(AGMO):c.842dup (p.Trp282MetfsTer13)
Gene: AGMO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.15387521dup , CM000669.2:g.15387521dup GRCh38
NC_000007.13:g.15427146dup , CM000669.1:g.15427146dup GRCh37
NC_000007.12:g.15393671dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001004320.2:c.842dup MANE Select NP_001004320.1:p.Trp282MetfsTer13
ENST00000342526.8:c.842dup MANE Select ENSP00000341662.3:p.Trp282MetfsTer13
NM_001004320.1:c.842dup NP_001004320.1:p.Trp282MetfsTer13
ENST00000342526.7:c.842dup ENSP00000341662.3:p.Trp282MetfsTer13
XM_006715730.1:c.842dup XP_006715793.1:p.Trp282MetfsTer13
XM_006715731.2:c.842dup XP_006715794.1:p.Trp282MetfsTer13
XM_006715731.3:c.842dup XP_006715794.1:p.Trp282MetfsTer13
XM_011515402.1:c.842dup XP_011513704.1:p.Trp282MetfsTer13
XM_011515402.3:c.842dup XP_011513704.1:p.Trp282MetfsTer13
XM_011515403.1:c.776dup XP_011513705.1:p.Trp260MetfsTer13
XM_017012204.1:c.842dup XP_016867693.1:p.Trp282MetfsTer13
XR_001744759.1:n.1012dup