Canonical Allele Identifier: CA2497275517
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1846067512
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674726del , CM000671.2:g.136674726del GRCh38
NC_000009.11:g.139569178del , CM000671.1:g.139569178del GRCh37
NC_000009.10:g.138688999del NCBI36
NG_008090.1:g.17734del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.661+9del MANE Select ENSP00000360761.2:n.661+9del
ENST00000371694.7:c.565+9del ENSP00000360759.3:n.565+9del
ENST00000371696.6:c.661+9del ENSP00000360761.2:n.661+9del
ENST00000472820.1:n.589+9del
ENST00000538402.1:c.661+9del ENSP00000438919.1:n.661+9del
NM_001012727.1:c.565+9del NP_001012745.1:n.565+9del
NM_006412.3:c.661+9del NP_006403.2:n.661+9del
NM_006412.4:c.661+9del MANE Select NP_006403.2:n.661+9del
NM_001012727.2:c.565+9del NP_001012745.1:n.565+9del
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