Canonical Allele Identifier: CA5342958

Gene: AGPAT2

Linked Data

• dbSNP Id: rs775264169
• ExAC: 9:139571140 G / GATCTGC
• gnomAD v2: 9-139571140-G-GATCTGC
• gnomAD v4: 9-136676688-G-GATCTGC
• MyVariant Identifiers: chr9:g.139571140_139571141insATCTGC (hg19) ; chr9:g.136676688_136676689insATCTGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676689_136676690insTCTGCA , CM000671.2:g.136676689_136676690insTCTGCA	GRCh38
NC_000009.11:g.139571141_139571142insTCTGCA , CM000671.1:g.139571141_139571142insTCTGCA	GRCh37
NC_000009.10:g.138690962_138690963insTCTGCA	NCBI36
NG_008090.1:g.15771_15772insGCAGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.493-9_493-8insGCAGAT MANE Select	ENSP00000360761.2:n.493-9_493-8insGCAGAT
ENST00000371694.7:c.492+272_492+273insGCAGAT	ENSP00000360759.3:n.492+272_492+273insGCAGAT
ENST00000371696.6:c.493-9_493-8insGCAGAT	ENSP00000360761.2:n.493-9_493-8insGCAGAT
ENST00000472820.1:n.421-9_421-8insGCAGAT
ENST00000538402.1:c.493-9_493-8insGCAGAT	ENSP00000438919.1:n.493-9_493-8insGCAGAT
NM_001012727.1:c.492+272_492+273insGCAGAT	NP_001012745.1:n.492+272_492+273insGCAGAT
NM_006412.3:c.493-9_493-8insGCAGAT	NP_006403.2:n.493-9_493-8insGCAGAT
NM_006412.4:c.493-9_493-8insGCAGAT MANE Select	NP_006403.2:n.493-9_493-8insGCAGAT
NM_001012727.2:c.492+272_492+273insGCAGAT	NP_001012745.1:n.492+272_492+273insGCAGAT