Canonical Allele Identifier: CA2786278289

Gene: AGPAT2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676935_136676936insCCCCCCCCCCCCCCCC , CM000671.2:g.136676935_136676936insCCCCCCCCCCCCCCCC	GRCh38
NC_000009.11:g.139571387_139571388insCCCCCCCCCCCCCCCC , CM000671.1:g.139571387_139571388insCCCCCCCCCCCCCCCC	GRCh37
NC_000009.10:g.138691208_138691209insCCCCCCCCCCCCCCCC	NCBI36
NG_008090.1:g.15528_15529insGGGGGGGGGGGGGGGG

Transcript Alleles

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