Canonical Allele Identifier: CA375578533

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136674765-A-T
• MyVariant Identifiers: chr9:g.139569217A>T (hg19) ; chr9:g.136674765A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674765A>T , CM000671.2:g.136674765A>T	GRCh38
NC_000009.11:g.139569217A>T , CM000671.1:g.139569217A>T	GRCh37
NC_000009.10:g.138689038A>T	NCBI36
NG_008090.1:g.17695T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.631T>A MANE Select	ENSP00000360761.2:p.Tyr211Asn
ENST00000371694.7:c.535T>A	ENSP00000360759.3:p.Tyr179Asn
ENST00000371696.6:c.631T>A	ENSP00000360761.2:p.Tyr211Asn
ENST00000472820.1:n.559T>A
ENST00000538402.1:c.631T>A	ENSP00000438919.1:p.Tyr211Asn
NM_001012727.1:c.535T>A	NP_001012745.1:p.Tyr179Asn
NM_006412.3:c.631T>A	NP_006403.2:p.Tyr211Asn
NM_006412.4:c.631T>A MANE Select	NP_006403.2:p.Tyr211Asn
NM_001012727.2:c.535T>A	NP_001012745.1:p.Tyr179Asn