Canonical Allele Identifier: CA2692654288
Gene: AGPAT2 HGNC NCBI

Linked Data

gnomAD v4: 9-136674847-A-AC
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674848dup , CM000671.2:g.136674848dup GRCh38
NC_000009.11:g.139569300dup , CM000671.1:g.139569300dup GRCh37
NC_000009.10:g.138689121dup NCBI36
NG_008090.1:g.17612dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.589-41dup MANE Select ENSP00000360761.2:n.589-41dup
ENST00000371694.7:c.493-41dup ENSP00000360759.3:n.493-41dup
ENST00000371696.6:c.589-41dup ENSP00000360761.2:n.589-41dup
ENST00000472820.1:n.517-41dup
ENST00000538402.1:c.589-41dup ENSP00000438919.1:n.589-41dup
NM_001012727.1:c.493-41dup NP_001012745.1:n.493-41dup
NM_006412.3:c.589-41dup NP_006403.2:n.589-41dup
NM_006412.4:c.589-41dup MANE Select NP_006403.2:n.589-41dup
NM_001012727.2:c.493-41dup NP_001012745.1:n.493-41dup
Search 100 bp 5'
Search 100 bp 3'