Canonical Allele Identifier: CA375578622

Gene: AGPAT2

Linked Data

• MyVariant Identifiers: chr9:g.139569228A>T (hg19) ; chr9:g.136674776A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674776A>T , CM000671.2:g.136674776A>T	GRCh38
NC_000009.11:g.139569228A>T , CM000671.1:g.139569228A>T	GRCh37
NC_000009.10:g.138689049A>T	NCBI36
NG_008090.1:g.17684T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371696.7:c.620T>A MANE Select	ENSP00000360761.2:p.Phe207Tyr
ENST00000371694.7:c.524T>A	ENSP00000360759.3:p.Phe175Tyr
ENST00000371696.6:c.620T>A	ENSP00000360761.2:p.Phe207Tyr
ENST00000472820.1:n.548T>A
ENST00000538402.1:c.620T>A	ENSP00000438919.1:p.Phe207Tyr
NM_001012727.1:c.524T>A	NP_001012745.1:p.Phe175Tyr
NM_006412.3:c.620T>A	NP_006403.2:p.Phe207Tyr
NM_006412.4:c.620T>A MANE Select	NP_006403.2:p.Phe207Tyr
NM_001012727.2:c.524T>A	NP_001012745.1:p.Phe175Tyr