Canonical Allele Identifier: CA467738296

Gene: AGPAT2

Linked Data

• MyVariant Identifiers: chr9:g.139569242C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674790C>G , CM000671.2:g.136674790C>G	GRCh38
NC_000009.11:g.139569242C>G , CM000671.1:g.139569242C>G	GRCh37
NC_000009.10:g.138689063C>G	NCBI36
NG_008090.1:g.17670G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.606G>C MANE Select	ENSP00000360761.2:p.Val202=
ENST00000371694.7:c.510G>C	ENSP00000360759.3:p.Val170=
ENST00000371696.6:c.606G>C	ENSP00000360761.2:p.Val202=
ENST00000472820.1:n.534G>C
ENST00000538402.1:c.606G>C	ENSP00000438919.1:p.Val202=
NM_001012727.1:c.510G>C	NP_001012745.1:p.Val170=
NM_006412.3:c.606G>C	NP_006403.2:p.Val202=
NM_006412.4:c.606G>C MANE Select	NP_006403.2:p.Val202=
NM_001012727.2:c.510G>C	NP_001012745.1:p.Val170=