Canonical Allele Identifier: CA2692654784

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136676908-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676908_136676909insT , CM000671.2:g.136676908_136676909insT	GRCh38
NC_000009.11:g.139571360_139571361insT , CM000671.1:g.139571360_139571361insT	GRCh37
NC_000009.10:g.138691181_138691182insT	NCBI36
NG_008090.1:g.15551_15552insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.492+52_492+53insA MANE Select	ENSP00000360761.2:n.492+52_492+53insA
ENST00000371694.7:c.492+52_492+53insA	ENSP00000360759.3:n.492+52_492+53insA
ENST00000371696.6:c.492+52_492+53insA	ENSP00000360761.2:n.492+52_492+53insA
ENST00000472820.1:n.420+52_420+53insA
ENST00000538402.1:c.492+52_492+53insA	ENSP00000438919.1:n.492+52_492+53insA
NM_001012727.1:c.492+52_492+53insA	NP_001012745.1:n.492+52_492+53insA
NM_006412.3:c.492+52_492+53insA	NP_006403.2:n.492+52_492+53insA
NM_006412.4:c.492+52_492+53insA MANE Select	NP_006403.2:n.492+52_492+53insA
NM_001012727.2:c.492+52_492+53insA	NP_001012745.1:n.492+52_492+53insA