Canonical Allele Identifier: CA2692654847

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136676931-A-ACCCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676935_136676936insCCCCC , CM000671.2:g.136676935_136676936insCCCCC	GRCh38
NC_000009.11:g.139571387_139571388insCCCCC , CM000671.1:g.139571387_139571388insCCCCC	GRCh37
NC_000009.10:g.138691208_138691209insCCCCC	NCBI36
NG_008090.1:g.15528_15529insGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.492+29_492+30insGGGGG MANE Select	ENSP00000360761.2:n.492+29_492+30insGGGGG
ENST00000371694.7:c.492+29_492+30insGGGGG	ENSP00000360759.3:n.492+29_492+30insGGGGG
ENST00000371696.6:c.492+29_492+30insGGGGG	ENSP00000360761.2:n.492+29_492+30insGGGGG
ENST00000472820.1:n.420+29_420+30insGGGGG
ENST00000538402.1:c.492+29_492+30insGGGGG	ENSP00000438919.1:n.492+29_492+30insGGGGG
NM_001012727.1:c.492+29_492+30insGGGGG	NP_001012745.1:n.492+29_492+30insGGGGG
NM_006412.3:c.492+29_492+30insGGGGG	NP_006403.2:n.492+29_492+30insGGGGG
NM_006412.4:c.492+29_492+30insGGGGG MANE Select	NP_006403.2:n.492+29_492+30insGGGGG
NM_001012727.2:c.492+29_492+30insGGGGG	NP_001012745.1:n.492+29_492+30insGGGGG