Canonical Allele Identifier: CA591367832

Gene: AGPAT2

Linked Data

• gnomAD v2: 9-139571372-G-GCCCCCC
• MyVariant Identifiers: chr9:g.139571372_139571373insCCCCCC (hg19) ; chr9:g.136676920_136676921insCCCCCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676924_136676925insCCCCCC , CM000671.2:g.136676924_136676925insCCCCCC	GRCh38
NC_000009.11:g.139571376_139571377insCCCCCC , CM000671.1:g.139571376_139571377insCCCCCC	GRCh37
NC_000009.10:g.138691197_138691198insCCCCCC	NCBI36
NG_008090.1:g.15539_15540insGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.492+40_492+41insGGGGGG MANE Select	ENSP00000360761.2:n.492+40_492+41insGGGGGG
ENST00000371694.7:c.492+40_492+41insGGGGGG	ENSP00000360759.3:n.492+40_492+41insGGGGGG
ENST00000371696.6:c.492+40_492+41insGGGGGG	ENSP00000360761.2:n.492+40_492+41insGGGGGG
ENST00000472820.1:n.420+40_420+41insGGGGGG
ENST00000538402.1:c.492+40_492+41insGGGGGG	ENSP00000438919.1:n.492+40_492+41insGGGGGG
NM_001012727.1:c.492+40_492+41insGGGGGG	NP_001012745.1:n.492+40_492+41insGGGGGG
NM_006412.3:c.492+40_492+41insGGGGGG	NP_006403.2:n.492+40_492+41insGGGGGG
NM_006412.4:c.492+40_492+41insGGGGGG MANE Select	NP_006403.2:n.492+40_492+41insGGGGGG
NM_001012727.2:c.492+40_492+41insGGGGGG	NP_001012745.1:n.492+40_492+41insGGGGGG