Canonical Allele Identifier: CA467744113

Gene: AGPAT2

Linked Data

• MyVariant Identifiers: chr9:g.139581732G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136687280G>A , CM000671.2:g.136687280G>A	GRCh38
NC_000009.11:g.139581732G>A , CM000671.1:g.139581732G>A	GRCh37
NC_000009.10:g.138701553G>A	NCBI36
NG_008090.1:g.5180C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.78C>T MANE Select	ENSP00000360761.2:p.Phe26=
ENST00000371694.7:c.78C>T	ENSP00000360759.3:p.Phe26=
ENST00000371696.6:c.78C>T	ENSP00000360761.2:p.Phe26=
ENST00000470861.1:n.86C>T
ENST00000538402.1:c.78C>T	ENSP00000438919.1:p.Phe26=
NM_001012727.1:c.78C>T	NP_001012745.1:p.Phe26=
NM_006412.3:c.78C>T	NP_006403.2:p.Phe26=
NM_006412.4:c.78C>T MANE Select	NP_006403.2:p.Phe26=
NM_001012727.2:c.78C>T	NP_001012745.1:p.Phe26=