Canonical Allele Identifier: CA2692653725
Gene: AGPAT2 HGNC NCBI

Linked Data

gnomAD v4: 9-136673735-C-CA
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673735_136673736insA , CM000671.2:g.136673735_136673736insA GRCh38
NC_000009.11:g.139568187_139568188insA , CM000671.1:g.139568187_139568188insA GRCh37
NC_000009.10:g.138688008_138688009insA NCBI36
NG_008090.1:g.18724_18725insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.*16_*17insT MANE Select ENSP00000360761.2:n.*16_*17insT
ENST00000371694.7:c.*16_*17insT ENSP00000360759.3:n.*16_*17insT
ENST00000371696.6:c.*16_*17insT ENSP00000360761.2:n.*16_*17insT
ENST00000472820.1:n.781_782insT
ENST00000538402.1:c.*16_*17insT ENSP00000438919.1:n.*16_*17insT
NM_001012727.1:c.*16_*17insT NP_001012745.1:n.*16_*17insT
NM_006412.3:c.*16_*17insT NP_006403.2:n.*16_*17insT
NM_006412.4:c.*16_*17insT MANE Select NP_006403.2:n.*16_*17insT
NM_001012727.2:c.*16_*17insT NP_001012745.1:n.*16_*17insT
Search 100 bp 5'
Search 100 bp 3'