Canonical Allele Identifier: CA375578965

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136674803-G-A
• MyVariant Identifiers: chr9:g.139569255G>A (hg19) ; chr9:g.136674803G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674803G>A , CM000671.2:g.136674803G>A	GRCh38
NC_000009.11:g.139569255G>A , CM000671.1:g.139569255G>A	GRCh37
NC_000009.10:g.138689076G>A	NCBI36
NG_008090.1:g.17657C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.593C>T MANE Select	ENSP00000360761.2:p.Pro198Leu
ENST00000371694.7:c.497C>T	ENSP00000360759.3:p.Pro166Leu
ENST00000371696.6:c.593C>T	ENSP00000360761.2:p.Pro198Leu
ENST00000472820.1:n.521C>T
ENST00000538402.1:c.593C>T	ENSP00000438919.1:p.Pro198Leu
NM_001012727.1:c.497C>T	NP_001012745.1:p.Pro166Leu
NM_006412.3:c.593C>T	NP_006403.2:p.Pro198Leu
NM_006412.4:c.593C>T MANE Select	NP_006403.2:p.Pro198Leu
NM_001012727.2:c.497C>T	NP_001012745.1:p.Pro166Leu