Canonical Allele Identifier: CA375578123

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136674735-C-A
• MyVariant Identifiers: chr9:g.139569187C>A (hg19) ; chr9:g.136674735C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674735C>A , CM000671.2:g.136674735C>A	GRCh38
NC_000009.11:g.139569187C>A , CM000671.1:g.139569187C>A	GRCh37
NC_000009.10:g.138689008C>A	NCBI36
NG_008090.1:g.17725G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.661G>T MANE Select	ENSP00000360761.2:p.Gly221Ter
ENST00000371694.7:c.565G>T	ENSP00000360759.3:p.Gly189Ter
ENST00000371696.6:c.661G>T	ENSP00000360761.2:p.Gly221Ter
ENST00000472820.1:n.589G>T
ENST00000538402.1:c.661G>T	ENSP00000438919.1:p.Gly221Ter
NM_001012727.1:c.565G>T	NP_001012745.1:p.Gly189Ter
NM_006412.3:c.661G>T	NP_006403.2:p.Gly221Ter
NM_006412.4:c.661G>T MANE Select	NP_006403.2:p.Gly221Ter
NM_001012727.2:c.565G>T	NP_001012745.1:p.Gly189Ter