Canonical Allele Identifier: CA2692654837

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136676928-CCAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676930_136676932del , CM000671.2:g.136676930_136676932del	GRCh38
NC_000009.11:g.139571382_139571384del , CM000671.1:g.139571382_139571384del	GRCh37
NC_000009.10:g.138691203_138691205del	NCBI36
NG_008090.1:g.15529_15531del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.492+30_492+32del MANE Select	ENSP00000360761.2:n.492+30_492+32del
ENST00000371694.7:c.492+30_492+32del	ENSP00000360759.3:n.492+30_492+32del
ENST00000371696.6:c.492+30_492+32del	ENSP00000360761.2:n.492+30_492+32del
ENST00000472820.1:n.420+30_420+32del
ENST00000538402.1:c.492+30_492+32del	ENSP00000438919.1:n.492+30_492+32del
NM_001012727.1:c.492+30_492+32del	NP_001012745.1:n.492+30_492+32del
NM_006412.3:c.492+30_492+32del	NP_006403.2:n.492+30_492+32del
NM_006412.4:c.492+30_492+32del MANE Select	NP_006403.2:n.492+30_492+32del
NM_001012727.2:c.492+30_492+32del	NP_001012745.1:n.492+30_492+32del