Canonical Allele Identifier: CA375577646

Gene: AGPAT2

Linked Data

• MyVariant Identifiers: chr9:g.139568350T>G (hg19) ; chr9:g.136673898T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136673898T>G , CM000671.2:g.136673898T>G	GRCh38
NC_000009.11:g.139568350T>G , CM000671.1:g.139568350T>G	GRCh37
NC_000009.10:g.138688171T>G	NCBI36
NG_008090.1:g.18562A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.691A>C MANE Select	ENSP00000360761.2:p.Ile231Leu
ENST00000371694.7:c.595A>C	ENSP00000360759.3:p.Ile199Leu
ENST00000371696.6:c.691A>C	ENSP00000360761.2:p.Ile231Leu
ENST00000472820.1:n.619A>C
ENST00000538402.1:c.691A>C	ENSP00000438919.1:p.Ile231Leu
NM_001012727.1:c.595A>C	NP_001012745.1:p.Ile199Leu
NM_006412.3:c.691A>C	NP_006403.2:p.Ile231Leu
NM_006412.4:c.691A>C MANE Select	NP_006403.2:p.Ile231Leu
NM_001012727.2:c.595A>C	NP_001012745.1:p.Ile199Leu