Canonical Allele Identifier: CA1690355652
Gene: AGMO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.15451358C>G , CM000669.2:g.15451358C>G GRCh38
NC_000007.13:g.15490983C>G , CM000669.1:g.15490983C>G GRCh37
NC_000007.12:g.15457508C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000342526.8:c.410-20250G>C MANE Select ENSP00000341662.3:n.410-20250G>C
ENST00000342526.7:c.410-20250G>C ENSP00000341662.3:n.410-20250G>C
NM_001004320.1:c.410-20250G>C NP_001004320.1:n.410-20250G>C
XM_006715730.1:c.410-20250G>C XP_006715793.1:n.410-20250G>C
XM_006715731.2:c.410-20250G>C XP_006715794.1:n.410-20250G>C
XM_011515402.1:c.410-20250G>C XP_011513704.1:n.410-20250G>C
XM_011515403.1:c.410-20250G>C XP_011513705.1:n.410-20250G>C
XM_006715731.3:c.410-20250G>C XP_006715794.1:n.410-20250G>C
XM_011515402.3:c.410-20250G>C XP_011513704.1:n.410-20250G>C
XM_017012204.1:c.410-20250G>C XP_016867693.1:n.410-20250G>C
XR_001744759.1:n.580-20250G>C
NM_001004320.2:c.410-20250G>C MANE Select NP_001004320.1:n.410-20250G>C