Canonical Allele Identifier: CA591367876

Gene: AGPAT2

Linked Data

• dbSNP Id: rs1296611107
• gnomAD v2: 9-139581614-GC-G
• gnomAD v4: 9-136687162-GC-G
• MyVariant Identifiers: chr9:g.139581615del (hg19) ; chr9:g.136687163del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136687167del , CM000671.2:g.136687167del	GRCh38
NC_000009.11:g.139581619del , CM000671.1:g.139581619del	GRCh37
NC_000009.10:g.138701440del	NCBI36
NG_008090.1:g.5297del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.182+13del MANE Select	ENSP00000360761.2:n.182+13del
ENST00000371694.7:c.182+13del	ENSP00000360759.3:n.182+13del
ENST00000371696.6:c.182+13del	ENSP00000360761.2:n.182+13del
ENST00000470861.1:n.190+13del
ENST00000538402.1:c.182+13del	ENSP00000438919.1:n.182+13del
NM_001012727.1:c.182+13del	NP_001012745.1:n.182+13del
NM_006412.3:c.182+13del	NP_006403.2:n.182+13del
NM_006412.4:c.182+13del MANE Select	NP_006403.2:n.182+13del
NM_001012727.2:c.182+13del	NP_001012745.1:n.182+13del