Canonical Allele Identifier: CA2786280005
Gene: AGPAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136676562dup , CM000671.2:g.136676562dup GRCh38
NC_000009.11:g.139571014dup , CM000671.1:g.139571014dup GRCh37
NC_000009.10:g.138690835dup NCBI36
NG_008090.1:g.15898dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.588+23dup MANE Select ENSP00000360761.2:n.588+23dup
ENST00000371694.7:c.492+399dup ENSP00000360759.3:n.492+399dup
ENST00000371696.6:c.588+23dup ENSP00000360761.2:n.588+23dup
ENST00000472820.1:n.516+23dup
ENST00000538402.1:c.588+23dup ENSP00000438919.1:n.588+23dup
NM_001012727.1:c.492+399dup NP_001012745.1:n.492+399dup
NM_006412.3:c.588+23dup NP_006403.2:n.588+23dup
NM_006412.4:c.588+23dup MANE Select NP_006403.2:n.588+23dup
NM_001012727.2:c.492+399dup NP_001012745.1:n.492+399dup