Canonical Allele Identifier: CA5342824

Gene: AGPAT2

Linked Data

• dbSNP Id: rs764643486
• ExAC: 9:139568273 G / T
• gnomAD v2: 9-139568273-G-T
• gnomAD v3: 9-136673821-G-T
• gnomAD v4: 9-136673821-G-T
• MyVariant Identifiers: chr9:g.139568273G>T (hg19) ; chr9:g.136673821G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136673821G>T , CM000671.2:g.136673821G>T	GRCh38
NC_000009.11:g.139568273G>T , CM000671.1:g.139568273G>T	GRCh37
NC_000009.10:g.138688094G>T	NCBI36
NG_008090.1:g.18639C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371696.7:c.768C>A MANE Select	ENSP00000360761.2:p.Phe256Leu
ENST00000371694.7:c.672C>A	ENSP00000360759.3:p.Phe224Leu
ENST00000371696.6:c.768C>A	ENSP00000360761.2:p.Phe256Leu
ENST00000472820.1:n.696C>A
ENST00000538402.1:c.768C>A	ENSP00000438919.1:p.Phe256Leu
NM_001012727.1:c.672C>A	NP_001012745.1:p.Phe224Leu
NM_006412.3:c.768C>A	NP_006403.2:p.Phe256Leu
NM_006412.4:c.768C>A MANE Select	NP_006403.2:p.Phe256Leu
NM_001012727.2:c.672C>A	NP_001012745.1:p.Phe224Leu