Canonical Allele Identifier: CA2692654805

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136676914-G-GCCTTCT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676916_136676917insTTCTCC , CM000671.2:g.136676916_136676917insTTCTCC	GRCh38
NC_000009.11:g.139571368_139571369insTTCTCC , CM000671.1:g.139571368_139571369insTTCTCC	GRCh37
NC_000009.10:g.138691189_138691190insTTCTCC	NCBI36
NG_008090.1:g.15545_15546insAGAAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.492+46_492+47insAGAAGG MANE Select	ENSP00000360761.2:n.492+46_492+47insAGAAGG
ENST00000371694.7:c.492+46_492+47insAGAAGG	ENSP00000360759.3:n.492+46_492+47insAGAAGG
ENST00000371696.6:c.492+46_492+47insAGAAGG	ENSP00000360761.2:n.492+46_492+47insAGAAGG
ENST00000472820.1:n.420+46_420+47insAGAAGG
ENST00000538402.1:c.492+46_492+47insAGAAGG	ENSP00000438919.1:n.492+46_492+47insAGAAGG
NM_001012727.1:c.492+46_492+47insAGAAGG	NP_001012745.1:n.492+46_492+47insAGAAGG
NM_006412.3:c.492+46_492+47insAGAAGG	NP_006403.2:n.492+46_492+47insAGAAGG
NM_006412.4:c.492+46_492+47insAGAAGG MANE Select	NP_006403.2:n.492+46_492+47insAGAAGG
NM_001012727.2:c.492+46_492+47insAGAAGG	NP_001012745.1:n.492+46_492+47insAGAAGG