Canonical Allele Identifier: CA375578359

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136674755-T-C
• MyVariant Identifiers: chr9:g.139569207T>C (hg19) ; chr9:g.136674755T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674755T>C , CM000671.2:g.136674755T>C	GRCh38
NC_000009.11:g.139569207T>C , CM000671.1:g.139569207T>C	GRCh37
NC_000009.10:g.138689028T>C	NCBI36
NG_008090.1:g.17705A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371696.7:c.641A>G MANE Select	ENSP00000360761.2:p.Lys214Arg
ENST00000371694.7:c.545A>G	ENSP00000360759.3:p.Lys182Arg
ENST00000371696.6:c.641A>G	ENSP00000360761.2:p.Lys214Arg
ENST00000472820.1:n.569A>G
ENST00000538402.1:c.641A>G	ENSP00000438919.1:p.Lys214Arg
NM_001012727.1:c.545A>G	NP_001012745.1:p.Lys182Arg
NM_006412.3:c.641A>G	NP_006403.2:p.Lys214Arg
NM_006412.4:c.641A>G MANE Select	NP_006403.2:p.Lys214Arg
NM_001012727.2:c.545A>G	NP_001012745.1:p.Lys182Arg