Canonical Allele Identifier: CA2692654804

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136676914-G-GCCCCCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676917_136676918insCCCCCCC , CM000671.2:g.136676917_136676918insCCCCCCC	GRCh38
NC_000009.11:g.139571369_139571370insCCCCCCC , CM000671.1:g.139571369_139571370insCCCCCCC	GRCh37
NC_000009.10:g.138691190_138691191insCCCCCCC	NCBI36
NG_008090.1:g.15545_15546insGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.492+46_492+47insGGGGGGG MANE Select	ENSP00000360761.2:n.492+46_492+47insGGGGGGG
ENST00000371694.7:c.492+46_492+47insGGGGGGG	ENSP00000360759.3:n.492+46_492+47insGGGGGGG
ENST00000371696.6:c.492+46_492+47insGGGGGGG	ENSP00000360761.2:n.492+46_492+47insGGGGGGG
ENST00000472820.1:n.420+46_420+47insGGGGGGG
ENST00000538402.1:c.492+46_492+47insGGGGGGG	ENSP00000438919.1:n.492+46_492+47insGGGGGGG
NM_001012727.1:c.492+46_492+47insGGGGGGG	NP_001012745.1:n.492+46_492+47insGGGGGGG
NM_006412.3:c.492+46_492+47insGGGGGGG	NP_006403.2:n.492+46_492+47insGGGGGGG
NM_006412.4:c.492+46_492+47insGGGGGGG MANE Select	NP_006403.2:n.492+46_492+47insGGGGGGG
NM_001012727.2:c.492+46_492+47insGGGGGGG	NP_001012745.1:n.492+46_492+47insGGGGGGG