Canonical Allele Identifier: CA2497275501
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1846040351

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673619_136673625dup , CM000671.2:g.136673619_136673625dup GRCh38
NC_000009.11:g.139568071_139568077dup , CM000671.1:g.139568071_139568077dup GRCh37
NC_000009.10:g.138687892_138687898dup NCBI36
NG_008090.1:g.18836_18842dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.*128_*134dup MANE Select ENSP00000360761.2:n.*128_*134dup
ENST00000371694.7:c.*128_*134dup ENSP00000360759.3:n.*128_*134dup
ENST00000371696.6:c.*128_*134dup ENSP00000360761.2:n.*128_*134dup
ENST00000538402.1:c.*128_*134dup ENSP00000438919.1:n.*128_*134dup
NM_001012727.1:c.*128_*134dup NP_001012745.1:n.*128_*134dup
NM_006412.3:c.*128_*134dup NP_006403.2:n.*128_*134dup
NM_006412.4:c.*128_*134dup MANE Select NP_006403.2:n.*128_*134dup
NM_001012727.2:c.*128_*134dup NP_001012745.1:n.*128_*134dup