Canonical Allele Identifier: CA861089457
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1379772727

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687260_136687261del , CM000671.2:g.136687260_136687261del GRCh38
NC_000009.11:g.139581712_139581713del , CM000671.1:g.139581712_139581713del GRCh37
NC_000009.10:g.138701533_138701534del NCBI36
NG_008090.1:g.5199_5200del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.97_98del MANE Select ENSP00000360761.2:p.Tyr33LeufsTer?
ENST00000371694.7:c.97_98del ENSP00000360759.3:p.Tyr33LeufsTer?
ENST00000371696.6:c.97_98del ENSP00000360761.2:p.Tyr33LeufsTer?
ENST00000470861.1:n.105_106del
ENST00000538402.1:c.97_98del ENSP00000438919.1:p.Tyr33LeufsTer?
NM_001012727.1:c.97_98del NP_001012745.1:p.Tyr33LeufsTer?
NM_006412.3:c.97_98del NP_006403.2:p.Tyr33LeufsTer?
NM_006412.4:c.97_98del MANE Select NP_006403.2:p.Tyr33LeufsTer?
NM_001012727.2:c.97_98del NP_001012745.1:p.Tyr33LeufsTer?