Canonical Allele Identifier: CA591184435

Gene: AGPAT2

Linked Data

• dbSNP Id: rs1314474828
• gnomAD v2: 9-139570602-C-CA
• gnomAD v3: 9-136676150-C-CA
• gnomAD v4: 9-136676150-C-CA
• MyVariant Identifiers: chr9:g.139570602_139570603insA (hg19) ; chr9:g.136676150_136676151insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676151dup , CM000671.2:g.136676151dup	GRCh38
NC_000009.11:g.139570603dup , CM000671.1:g.139570603dup	GRCh37
NC_000009.10:g.138690424dup	NCBI36
NG_008090.1:g.16309dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000371696.7:c.588+434dup MANE Select	ENSP00000360761.2:n.588+434dup
ENST00000371694.7:c.492+810dup	ENSP00000360759.3:n.492+810dup
ENST00000371696.6:c.588+434dup	ENSP00000360761.2:n.588+434dup
ENST00000472820.1:n.516+434dup
ENST00000538402.1:c.588+434dup	ENSP00000438919.1:n.588+434dup
NM_001012727.1:c.492+810dup	NP_001012745.1:n.492+810dup
NM_006412.3:c.588+434dup	NP_006403.2:n.588+434dup
NM_006412.4:c.588+434dup MANE Select	NP_006403.2:n.588+434dup
NM_001012727.2:c.492+810dup	NP_001012745.1:n.492+810dup