Canonical Allele Identifier: CA2692655270
Gene: AGPAT2 HGNC NCBI

Linked Data

gnomAD v4: 9-136687080-C-CT
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687080_136687081insT , CM000671.2:g.136687080_136687081insT GRCh38
NC_000009.11:g.139581532_139581533insT , CM000671.1:g.139581532_139581533insT GRCh37
NC_000009.10:g.138701353_138701354insT NCBI36
NG_008090.1:g.5379_5380insA

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.182+95_182+96insA MANE Select ENSP00000360761.2:n.182+95_182+96insA
ENST00000371694.7:c.182+95_182+96insA ENSP00000360759.3:n.182+95_182+96insA
ENST00000371696.6:c.182+95_182+96insA ENSP00000360761.2:n.182+95_182+96insA
ENST00000470861.1:n.190+95_190+96insA
ENST00000538402.1:c.182+95_182+96insA ENSP00000438919.1:n.182+95_182+96insA
NM_001012727.1:c.182+95_182+96insA NP_001012745.1:n.182+95_182+96insA
NM_006412.3:c.182+95_182+96insA NP_006403.2:n.182+95_182+96insA
NM_006412.4:c.182+95_182+96insA MANE Select NP_006403.2:n.182+95_182+96insA
NM_001012727.2:c.182+95_182+96insA NP_001012745.1:n.182+95_182+96insA
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