Canonical Allele Identifier: CA1130022086
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687300_136687304del , CM000671.2:g.136687300_136687304del GRCh38
NC_000009.11:g.139581752_139581756del , CM000671.1:g.139581752_139581756del GRCh37
NC_000009.10:g.138701573_138701577del NCBI36
NG_008090.1:g.5156_5160del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.54_58del MANE Select ENSP00000360761.2:p.Gln19GlufsTer?
ENST00000371694.7:c.54_58del ENSP00000360759.3:p.Gln19GlufsTer?
ENST00000371696.6:c.54_58del ENSP00000360761.2:p.Gln19GlufsTer?
ENST00000470861.1:n.62_66del
ENST00000538402.1:c.54_58del ENSP00000438919.1:p.Gln19GlufsTer?
NM_001012727.1:c.54_58del NP_001012745.1:p.Gln19GlufsTer?
NM_006412.3:c.54_58del NP_006403.2:p.Gln19GlufsTer?
NM_006412.4:c.54_58del MANE Select NP_006403.2:p.Gln19GlufsTer?
NM_001012727.2:c.54_58del NP_001012745.1:p.Gln19GlufsTer?