Canonical Allele Identifier: CA2692654851

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136676931-A-AACC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676931_136676932insACC , CM000671.2:g.136676931_136676932insACC	GRCh38
NC_000009.11:g.139571383_139571384insACC , CM000671.1:g.139571383_139571384insACC	GRCh37
NC_000009.10:g.138691204_138691205insACC	NCBI36
NG_008090.1:g.15528_15529insGGT

Transcript Alleles

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