Canonical Allele Identifier: CA1130033743
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1846068431

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674768dup , CM000671.2:g.136674768dup GRCh38
NC_000009.11:g.139569220dup , CM000671.1:g.139569220dup GRCh37
NC_000009.10:g.138689041dup NCBI36
NG_008090.1:g.17693dup

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.629dup MANE Select ENSP00000360761.2:p.Tyr211LeufsTer?
ENST00000371694.7:c.533dup ENSP00000360759.3:p.Tyr179LeufsTer?
ENST00000371696.6:c.629dup ENSP00000360761.2:p.Tyr211LeufsTer?
ENST00000472820.1:n.557dup
ENST00000538402.1:c.629dup ENSP00000438919.1:p.Tyr211LeufsTer?
NM_001012727.1:c.533dup NP_001012745.1:p.Tyr179LeufsTer?
NM_006412.3:c.629dup NP_006403.2:p.Tyr211LeufsTer?
NM_006412.4:c.629dup MANE Select NP_006403.2:p.Tyr211LeufsTer?
NM_001012727.2:c.533dup NP_001012745.1:p.Tyr179LeufsTer?