Canonical Allele Identifier: CA154043312

Gene: AGMO

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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