Canonical Allele Identifier: CA1690403287
Community Standard Title: NM_001004320.2(AGMO):c.409+58T=
Gene: AGMO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.15544714A= , CM000669.2:g.15544714A= GRCh38
NC_000007.13:g.15584339A= , CM000669.1:g.15584339A= GRCh37
NC_000007.12:g.15550864A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001004320.2:c.409+58T= MANE Select NP_001004320.1:n.409+58T=
ENST00000342526.8:c.409+58T= MANE Select ENSP00000341662.3:n.409+58T=
NM_001004320.1:c.409+58T= NP_001004320.1:n.409+58T=
ENST00000342526.7:c.409+58T= ENSP00000341662.3:n.409+58T=
XM_006715730.1:c.409+58T= XP_006715793.1:n.409+58T=
XM_006715731.2:c.409+58T= XP_006715794.1:n.409+58T=
XM_006715731.3:c.409+58T= XP_006715794.1:n.409+58T=
XM_011515402.1:c.409+58T= XP_011513704.1:n.409+58T=
XM_011515402.3:c.409+58T= XP_011513704.1:n.409+58T=
XM_011515403.1:c.409+58T= XP_011513705.1:n.409+58T=
XM_017012204.1:c.409+58T= XP_016867693.1:n.409+58T=
XR_001744759.1:n.579+58T=