Canonical Allele Identifier: CA2692654307
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674864del , CM000671.2:g.136674864del GRCh38
NC_000009.11:g.139569316del , CM000671.1:g.139569316del GRCh37
NC_000009.10:g.138689137del NCBI36
NG_008090.1:g.17599del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.589-54del MANE Select ENSP00000360761.2:n.589-54del
ENST00000371694.7:c.493-54del ENSP00000360759.3:n.493-54del
ENST00000371696.6:c.589-54del ENSP00000360761.2:n.589-54del
ENST00000472820.1:n.517-54del
ENST00000538402.1:c.589-54del ENSP00000438919.1:n.589-54del
NM_001012727.1:c.493-54del NP_001012745.1:n.493-54del
NM_006412.3:c.589-54del NP_006403.2:n.589-54del
NM_006412.4:c.589-54del MANE Select NP_006403.2:n.589-54del
NM_001012727.2:c.493-54del NP_001012745.1:n.493-54del