Canonical Allele Identifier: CA5342902

Gene: AGPAT2

Linked Data

• dbSNP Id: rs377267603
• ExAC: 9:139569219 A / G
• gnomAD v2: 9-139569219-A-G
• gnomAD v3: 9-136674767-A-G
• gnomAD v4: 9-136674767-A-G
• MyVariant Identifiers: chr9:g.139569219A>G (hg19) ; chr9:g.139569219_139569222delinsGAGG (hg19) ; chr9:g.136674767A>G (hg38) ; chr9:g.136674767_136674770delinsGAGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674767A>G , CM000671.2:g.136674767A>G	GRCh38
NC_000009.11:g.139569219A>G , CM000671.1:g.139569219A>G	GRCh37
NC_000009.10:g.138689040A>G	NCBI36
NG_008090.1:g.17693T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371696.7:c.629T>C MANE Select	ENSP00000360761.2:p.Phe210Ser
ENST00000371694.7:c.533T>C	ENSP00000360759.3:p.Phe178Ser
ENST00000371696.6:c.629T>C	ENSP00000360761.2:p.Phe210Ser
ENST00000472820.1:n.557T>C
ENST00000538402.1:c.629T>C	ENSP00000438919.1:p.Phe210Ser
NM_001012727.1:c.533T>C	NP_001012745.1:p.Phe178Ser
NM_006412.3:c.629T>C	NP_006403.2:p.Phe210Ser
NM_006412.4:c.629T>C MANE Select	NP_006403.2:p.Phe210Ser
NM_001012727.2:c.533T>C	NP_001012745.1:p.Phe178Ser