Canonical Allele Identifier: CA2692655439

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136687392-GCTCCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136687393_136687397del , CM000671.2:g.136687393_136687397del	GRCh38
NC_000009.11:g.139581845_139581849del , CM000671.1:g.139581845_139581849del	GRCh37
NC_000009.10:g.138701666_138701670del	NCBI36
NG_008090.1:g.5063_5067del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.-40_-36del MANE Select	ENSP00000360761.2:n.-40_-36del
ENST00000371694.7:c.-40_-36del	ENSP00000360759.3:n.-40_-36del
ENST00000371696.6:c.-40_-36del	ENSP00000360761.2:n.-40_-36del
NM_001012727.1:c.-40_-36del	NP_001012745.1:n.-40_-36del
NM_006412.3:c.-40_-36del	NP_006403.2:n.-40_-36del
NM_006412.4:c.-40_-36del MANE Select	NP_006403.2:n.-40_-36del
NM_001012727.2:c.-40_-36del	NP_001012745.1:n.-40_-36del