Canonical Allele Identifier: CA2692654792

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136676909-G-GCCCCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676913_136676914insCCCCCC , CM000671.2:g.136676913_136676914insCCCCCC	GRCh38
NC_000009.11:g.139571365_139571366insCCCCCC , CM000671.1:g.139571365_139571366insCCCCCC	GRCh37
NC_000009.10:g.138691186_138691187insCCCCCC	NCBI36
NG_008090.1:g.15550_15551insGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.492+51_492+52insGGGGGG MANE Select	ENSP00000360761.2:n.492+51_492+52insGGGGGG
ENST00000371694.7:c.492+51_492+52insGGGGGG	ENSP00000360759.3:n.492+51_492+52insGGGGGG
ENST00000371696.6:c.492+51_492+52insGGGGGG	ENSP00000360761.2:n.492+51_492+52insGGGGGG
ENST00000472820.1:n.420+51_420+52insGGGGGG
ENST00000538402.1:c.492+51_492+52insGGGGGG	ENSP00000438919.1:n.492+51_492+52insGGGGGG
NM_001012727.1:c.492+51_492+52insGGGGGG	NP_001012745.1:n.492+51_492+52insGGGGGG
NM_006412.3:c.492+51_492+52insGGGGGG	NP_006403.2:n.492+51_492+52insGGGGGG
NM_006412.4:c.492+51_492+52insGGGGGG MANE Select	NP_006403.2:n.492+51_492+52insGGGGGG
NM_001012727.2:c.492+51_492+52insGGGGGG	NP_001012745.1:n.492+51_492+52insGGGGGG