Canonical Allele Identifier: CA201623189

Gene: AGPAT2

Linked Data

• dbSNP Id: rs71675070
• gnomAD v2: 9-139567987-C-CGAGCCT
• gnomAD v3: 9-136673535-C-CGAGCCT
• gnomAD v4: 9-136673535-C-CGAGCCT
• MyVariant Identifiers: chr9:g.139567987_139567988insGAGCCT (hg19) ; chr9:g.136673535_136673536insGAGCCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136673540_136673541insTGAGCC , CM000671.2:g.136673540_136673541insTGAGCC	GRCh38
NC_000009.11:g.139567992_139567993insTGAGCC , CM000671.1:g.139567992_139567993insTGAGCC	GRCh37
NC_000009.10:g.138687813_138687814insTGAGCC	NCBI36
NG_008090.1:g.18924_18925insAGGCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.*216_*217insAGGCTC MANE Select	ENSP00000360761.2:n.*216_*217insAGGCTC
ENST00000371694.7:c.*216_*217insAGGCTC	ENSP00000360759.3:n.*216_*217insAGGCTC
ENST00000371696.6:c.*216_*217insAGGCTC	ENSP00000360761.2:n.*216_*217insAGGCTC
ENST00000538402.1:c.*216_*217insAGGCTC	ENSP00000438919.1:n.*216_*217insAGGCTC
NM_001012727.1:c.*216_*217insAGGCTC	NP_001012745.1:n.*216_*217insAGGCTC
NM_006412.3:c.*216_*217insAGGCTC	NP_006403.2:n.*216_*217insAGGCTC
NM_006412.4:c.*216_*217insAGGCTC MANE Select	NP_006403.2:n.*216_*217insAGGCTC
NM_001012727.2:c.*216_*217insAGGCTC	NP_001012745.1:n.*216_*217insAGGCTC