Canonical Allele Identifier: CA591183782

Gene: AGPAT2

Linked Data

• dbSNP Id: rs1402508389
• gnomAD v2: 9-139569270-G-GGA
• gnomAD v4: 9-136674818-G-GGA
• MyVariant Identifiers: chr9:g.139569270_139569271insGA (hg19) ; chr9:g.136674818_136674819insGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674821_136674822dup , CM000671.2:g.136674821_136674822dup	GRCh38
NC_000009.11:g.139569273_139569274dup , CM000671.1:g.139569273_139569274dup	GRCh37
NC_000009.10:g.138689094_138689095dup	NCBI36
NG_008090.1:g.17640_17641dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.589-13_589-12dup MANE Select	ENSP00000360761.2:n.589-13_589-12dup
ENST00000371694.7:c.493-13_493-12dup	ENSP00000360759.3:n.493-13_493-12dup
ENST00000371696.6:c.589-13_589-12dup	ENSP00000360761.2:n.589-13_589-12dup
ENST00000472820.1:n.517-13_517-12dup
ENST00000538402.1:c.589-13_589-12dup	ENSP00000438919.1:n.589-13_589-12dup
NM_001012727.1:c.493-13_493-12dup	NP_001012745.1:n.493-13_493-12dup
NM_006412.3:c.589-13_589-12dup	NP_006403.2:n.589-13_589-12dup
NM_006412.4:c.589-13_589-12dup MANE Select	NP_006403.2:n.589-13_589-12dup
NM_001012727.2:c.493-13_493-12dup	NP_001012745.1:n.493-13_493-12dup