Canonical Allele Identifier: CA2579519921
Gene: AGPAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674811dup , CM000671.2:g.136674811dup GRCh38
NC_000009.11:g.139569263dup , CM000671.1:g.139569263dup GRCh37
NC_000009.10:g.138689084dup NCBI36
NG_008090.1:g.17649dup

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.589-4dup MANE Select ENSP00000360761.2:n.589-4dup
ENST00000371694.7:c.493-4dup ENSP00000360759.3:n.493-4dup
ENST00000371696.6:c.589-4dup ENSP00000360761.2:n.589-4dup
ENST00000472820.1:n.517-4dup
ENST00000538402.1:c.589-4dup ENSP00000438919.1:n.589-4dup
NM_001012727.1:c.493-4dup NP_001012745.1:n.493-4dup
NM_006412.3:c.589-4dup NP_006403.2:n.589-4dup
NM_006412.4:c.589-4dup MANE Select NP_006403.2:n.589-4dup
NM_001012727.2:c.493-4dup NP_001012745.1:n.493-4dup