Canonical Allele Identifier: CA2497275643
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1846236502

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687330_136687334del , CM000671.2:g.136687330_136687334del GRCh38
NC_000009.11:g.139581782_139581786del , CM000671.1:g.139581782_139581786del GRCh37
NC_000009.10:g.138701603_138701607del NCBI36
NG_008090.1:g.5129_5133del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.27_31del MANE Select ENSP00000360761.2:p.Leu11ValfsTer?
ENST00000371694.7:c.27_31del ENSP00000360759.3:p.Leu11ValfsTer?
ENST00000371696.6:c.27_31del ENSP00000360761.2:p.Leu11ValfsTer?
ENST00000470861.1:n.35_39del
ENST00000538402.1:c.27_31del ENSP00000438919.1:p.Leu11ValfsTer?
NM_001012727.1:c.27_31del NP_001012745.1:p.Leu11ValfsTer?
NM_006412.3:c.27_31del NP_006403.2:p.Leu11ValfsTer?
NM_006412.4:c.27_31del MANE Select NP_006403.2:p.Leu11ValfsTer?
NM_001012727.2:c.27_31del NP_001012745.1:p.Leu11ValfsTer?