Canonical Allele Identifier: CA375577813

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136673927-C-A
• MyVariant Identifiers: chr9:g.139568379C>A (hg19) ; chr9:g.136673927C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136673927C>A , CM000671.2:g.136673927C>A	GRCh38
NC_000009.11:g.139568379C>A , CM000671.1:g.139568379C>A	GRCh37
NC_000009.10:g.138688200C>A	NCBI36
NG_008090.1:g.18533G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371696.7:c.662G>T MANE Select	ENSP00000360761.2:p.Gly221Val
ENST00000371694.7:c.566G>T	ENSP00000360759.3:p.Gly189Val
ENST00000371696.6:c.662G>T	ENSP00000360761.2:p.Gly221Val
ENST00000472820.1:n.590G>T
ENST00000538402.1:c.662G>T	ENSP00000438919.1:p.Gly221Val
NM_001012727.1:c.566G>T	NP_001012745.1:p.Gly189Val
NM_006412.3:c.662G>T	NP_006403.2:p.Gly221Val
NM_006412.4:c.662G>T MANE Select	NP_006403.2:p.Gly221Val
NM_001012727.2:c.566G>T	NP_001012745.1:p.Gly189Val