Canonical Allele Identifier: CA2497275515
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1846065068
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674617_136674618del , CM000671.2:g.136674617_136674618del GRCh38
NC_000009.11:g.139569069_139569070del , CM000671.1:g.139569069_139569070del GRCh37
NC_000009.10:g.138688890_138688891del NCBI36
NG_008090.1:g.17842_17843del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.661+117_661+118del MANE Select ENSP00000360761.2:n.661+117_661+118del
ENST00000371694.7:c.565+117_565+118del ENSP00000360759.3:n.565+117_565+118del
ENST00000371696.6:c.661+117_661+118del ENSP00000360761.2:n.661+117_661+118del
ENST00000472820.1:n.589+117_589+118del
ENST00000538402.1:c.661+117_661+118del ENSP00000438919.1:n.661+117_661+118del
NM_001012727.1:c.565+117_565+118del NP_001012745.1:n.565+117_565+118del
NM_006412.3:c.661+117_661+118del NP_006403.2:n.661+117_661+118del
NM_006412.4:c.661+117_661+118del MANE Select NP_006403.2:n.661+117_661+118del
NM_001012727.2:c.565+117_565+118del NP_001012745.1:n.565+117_565+118del
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