Canonical Allele Identifier: CA2692655479
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687419_136687420del , CM000671.2:g.136687419_136687420del GRCh38
NC_000009.11:g.139581871_139581872del , CM000671.1:g.139581871_139581872del GRCh37
NC_000009.10:g.138701692_138701693del NCBI36
NG_008090.1:g.5043_5044del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.-60_-59del MANE Select ENSP00000360761.2:n.-60_-59del
ENST00000371696.6:c.-60_-59del ENSP00000360761.2:n.-60_-59del
NM_001012727.1:c.-60_-59del NP_001012745.1:n.-60_-59del
NM_006412.3:c.-60_-59del NP_006403.2:n.-60_-59del
NM_006412.4:c.-60_-59del MANE Select NP_006403.2:n.-60_-59del
NM_001012727.2:c.-60_-59del NP_001012745.1:n.-60_-59del