Canonical Allele Identifier: CA2497275510
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1846052042

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674017dup , CM000671.2:g.136674017dup GRCh38
NC_000009.11:g.139568469dup , CM000671.1:g.139568469dup GRCh37
NC_000009.10:g.138688290dup NCBI36
NG_008090.1:g.18448dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.662-85dup MANE Select ENSP00000360761.2:n.662-85dup
ENST00000371694.7:c.566-85dup ENSP00000360759.3:n.566-85dup
ENST00000371696.6:c.662-85dup ENSP00000360761.2:n.662-85dup
ENST00000472820.1:n.590-85dup
ENST00000538402.1:c.662-85dup ENSP00000438919.1:n.662-85dup
NM_001012727.1:c.566-85dup NP_001012745.1:n.566-85dup
NM_006412.3:c.662-85dup NP_006403.2:n.662-85dup
NM_006412.4:c.662-85dup MANE Select NP_006403.2:n.662-85dup
NM_001012727.2:c.566-85dup NP_001012745.1:n.566-85dup