Canonical Allele Identifier: CA2692654399

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136674921-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674922del , CM000671.2:g.136674922del	GRCh38
NC_000009.11:g.139569374del , CM000671.1:g.139569374del	GRCh37
NC_000009.10:g.138689195del	NCBI36
NG_008090.1:g.17538del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.589-115del MANE Select	ENSP00000360761.2:n.589-115del
ENST00000371694.7:c.493-115del	ENSP00000360759.3:n.493-115del
ENST00000371696.6:c.589-115del	ENSP00000360761.2:n.589-115del
ENST00000472820.1:n.517-115del
ENST00000538402.1:c.589-115del	ENSP00000438919.1:n.589-115del
NM_001012727.1:c.493-115del	NP_001012745.1:n.493-115del
NM_006412.3:c.589-115del	NP_006403.2:n.589-115del
NM_006412.4:c.589-115del MANE Select	NP_006403.2:n.589-115del
NM_001012727.2:c.493-115del	NP_001012745.1:n.493-115del