Canonical Allele Identifier: CA5342899

Gene: AGPAT2

Linked Data

• dbSNP Id: rs754208307
• ExAC: 9:139569213 T / G
• gnomAD v2: 9-139569213-T-G
• gnomAD v3: 9-136674761-T-G
• gnomAD v4: 9-136674761-T-G
• MyVariant Identifiers: chr9:g.139569213T>G (hg19) ; chr9:g.136674761T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674761T>G , CM000671.2:g.136674761T>G	GRCh38
NC_000009.11:g.139569213T>G , CM000671.1:g.139569213T>G	GRCh37
NC_000009.10:g.138689034T>G	NCBI36
NG_008090.1:g.17699A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371696.7:c.635A>C MANE Select	ENSP00000360761.2:p.Asn212Thr
ENST00000371694.7:c.539A>C	ENSP00000360759.3:p.Asn180Thr
ENST00000371696.6:c.635A>C	ENSP00000360761.2:p.Asn212Thr
ENST00000472820.1:n.563A>C
ENST00000538402.1:c.635A>C	ENSP00000438919.1:p.Asn212Thr
NM_001012727.1:c.539A>C	NP_001012745.1:p.Asn180Thr
NM_006412.3:c.635A>C	NP_006403.2:p.Asn212Thr
NM_006412.4:c.635A>C MANE Select	NP_006403.2:p.Asn212Thr
NM_001012727.2:c.539A>C	NP_001012745.1:p.Asn180Thr