Canonical Allele Identifier: CA375588355

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136687309-G-T
• MyVariant Identifiers: chr9:g.139581761G>T (hg19) ; chr9:g.136687309G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136687309G>T , CM000671.2:g.136687309G>T	GRCh38
NC_000009.11:g.139581761G>T , CM000671.1:g.139581761G>T	GRCh37
NC_000009.10:g.138701582G>T	NCBI36
NG_008090.1:g.5151C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.49C>A MANE Select	ENSP00000360761.2:p.Leu17Met
ENST00000371694.7:c.49C>A	ENSP00000360759.3:p.Leu17Met
ENST00000371696.6:c.49C>A	ENSP00000360761.2:p.Leu17Met
ENST00000470861.1:n.57C>A
ENST00000538402.1:c.49C>A	ENSP00000438919.1:p.Leu17Met
NM_001012727.1:c.49C>A	NP_001012745.1:p.Leu17Met
NM_006412.3:c.49C>A	NP_006403.2:p.Leu17Met
NM_006412.4:c.49C>A MANE Select	NP_006403.2:p.Leu17Met
NM_001012727.2:c.49C>A	NP_001012745.1:p.Leu17Met