Canonical Allele Identifier: CA2692653613
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673652_136673674dup , CM000671.2:g.136673652_136673674dup GRCh38
NC_000009.11:g.139568104_139568126dup , CM000671.1:g.139568104_139568126dup GRCh37
NC_000009.10:g.138687925_138687947dup NCBI36
NG_008090.1:g.18792_18814dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.*84_*106dup MANE Select ENSP00000360761.2:n.*84_*106dup
ENST00000371694.7:c.*84_*106dup ENSP00000360759.3:n.*84_*106dup
ENST00000371696.6:c.*84_*106dup ENSP00000360761.2:n.*84_*106dup
ENST00000538402.1:c.*84_*106dup ENSP00000438919.1:n.*84_*106dup
NM_001012727.1:c.*84_*106dup NP_001012745.1:n.*84_*106dup
NM_006412.3:c.*84_*106dup NP_006403.2:n.*84_*106dup
NM_006412.4:c.*84_*106dup MANE Select NP_006403.2:n.*84_*106dup
NM_001012727.2:c.*84_*106dup NP_001012745.1:n.*84_*106dup