Canonical Allele Identifier: CA5343208

Gene: AGPAT2

Linked Data

• dbSNP Id: rs749110421
• ExAC: 9:139581843 C / CG
• gnomAD v2: 9-139581843-C-CG
• gnomAD v3: 9-136687391-C-CG
• gnomAD v4: 9-136687391-C-CG
• MyVariant Identifiers: chr9:g.139581843_139581844insG (hg19) ; chr9:g.136687391_136687392insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136687392dup , CM000671.2:g.136687392dup	GRCh38
NC_000009.11:g.139581844dup , CM000671.1:g.139581844dup	GRCh37
NC_000009.10:g.138701665dup	NCBI36
NG_008090.1:g.5068dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.-35dup MANE Select	ENSP00000360761.2:n.-35dup
ENST00000371694.7:c.-35dup	ENSP00000360759.3:n.-35dup
ENST00000371696.6:c.-35dup	ENSP00000360761.2:n.-35dup
ENST00000538402.1:c.-35dup	ENSP00000438919.1:n.-35dup
NM_001012727.1:c.-35dup	NP_001012745.1:n.-35dup
NM_006412.3:c.-35dup	NP_006403.2:n.-35dup
NM_006412.4:c.-35dup MANE Select	NP_006403.2:n.-35dup
NM_001012727.2:c.-35dup	NP_001012745.1:n.-35dup