Canonical Allele Identifier: CA2786279735
Gene: AGPAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687403_136687405del , CM000671.2:g.136687403_136687405del GRCh38
NC_000009.11:g.139581855_139581857del , CM000671.1:g.139581855_139581857del GRCh37
NC_000009.10:g.138701676_138701678del NCBI36
NG_008090.1:g.5056_5058del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.-47_-45del MANE Select ENSP00000360761.2:n.-47_-45del
ENST00000371696.6:c.-47_-45del ENSP00000360761.2:n.-47_-45del
NM_001012727.1:c.-47_-45del NP_001012745.1:n.-47_-45del
NM_006412.3:c.-47_-45del NP_006403.2:n.-47_-45del
NM_006412.4:c.-47_-45del MANE Select NP_006403.2:n.-47_-45del
NM_001012727.2:c.-47_-45del NP_001012745.1:n.-47_-45del