Canonical Allele Identifier: CA2692655263
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687080_136687093del , CM000671.2:g.136687080_136687093del GRCh38
NC_000009.11:g.139581532_139581545del , CM000671.1:g.139581532_139581545del GRCh37
NC_000009.10:g.138701353_138701366del NCBI36
NG_008090.1:g.5370_5383del

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.182+86_182+99del MANE Select ENSP00000360761.2:n.182+86_182+99del
ENST00000371694.7:c.182+86_182+99del ENSP00000360759.3:n.182+86_182+99del
ENST00000371696.6:c.182+86_182+99del ENSP00000360761.2:n.182+86_182+99del
ENST00000470861.1:n.190+86_190+99del
ENST00000538402.1:c.182+86_182+99del ENSP00000438919.1:n.182+86_182+99del
NM_001012727.1:c.182+86_182+99del NP_001012745.1:n.182+86_182+99del
NM_006412.3:c.182+86_182+99del NP_006403.2:n.182+86_182+99del
NM_006412.4:c.182+86_182+99del MANE Select NP_006403.2:n.182+86_182+99del
NM_001012727.2:c.182+86_182+99del NP_001012745.1:n.182+86_182+99del