Canonical Allele Identifier: CA2692653763
Gene: AGPAT2 HGNC NCBI

Linked Data

gnomAD v4: 9-136673862-CAGGGACG-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673863_136673869del , CM000671.2:g.136673863_136673869del GRCh38
NC_000009.11:g.139568315_139568321del , CM000671.1:g.139568315_139568321del GRCh37
NC_000009.10:g.138688136_138688142del NCBI36
NG_008090.1:g.18591_18597del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.720_726del MANE Select ENSP00000360761.2:p.Asp240GlufsTer11
ENST00000371694.7:c.624_630del ENSP00000360759.3:p.Asp208GlufsTer11
ENST00000371696.6:c.720_726del ENSP00000360761.2:p.Asp240GlufsTer11
ENST00000472820.1:n.648_654del
ENST00000538402.1:c.720_726del ENSP00000438919.1:p.Asp240GlufsTer11
NM_001012727.1:c.624_630del NP_001012745.1:p.Asp208GlufsTer11
NM_006412.3:c.720_726del NP_006403.2:p.Asp240GlufsTer11
NM_006412.4:c.720_726del MANE Select NP_006403.2:p.Asp240GlufsTer11
NM_001012727.2:c.624_630del NP_001012745.1:p.Asp208GlufsTer11
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