Canonical Allele Identifier: CA2692654229
Gene: AGPAT2 HGNC NCBI

Linked Data

gnomAD v4: 9-136674809-TGCAG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674815_136674818del , CM000671.2:g.136674815_136674818del GRCh38
NC_000009.11:g.139569267_139569270del , CM000671.1:g.139569267_139569270del GRCh37
NC_000009.10:g.138689088_138689091del NCBI36
NG_008090.1:g.17647_17650del

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.589-6_589-3del MANE Select ENSP00000360761.2:n.589-6_589-3del
ENST00000371694.7:c.493-6_493-3del ENSP00000360759.3:n.493-6_493-3del
ENST00000371696.6:c.589-6_589-3del ENSP00000360761.2:n.589-6_589-3del
ENST00000472820.1:n.517-6_517-3del
ENST00000538402.1:c.589-6_589-3del ENSP00000438919.1:n.589-6_589-3del
NM_001012727.1:c.493-6_493-3del NP_001012745.1:n.493-6_493-3del
NM_006412.3:c.589-6_589-3del NP_006403.2:n.589-6_589-3del
NM_006412.4:c.589-6_589-3del MANE Select NP_006403.2:n.589-6_589-3del
NM_001012727.2:c.493-6_493-3del NP_001012745.1:n.493-6_493-3del
Search 100 bp 5'
Search 100 bp 3'