Canonical Allele Identifier: CA2499899263
Gene: AGPAT2 HGNC NCBI

Linked Data

gnomAD v4: 9-136687074-G-GCGGGA
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687079_136687083dup , CM000671.2:g.136687079_136687083dup GRCh38
NC_000009.11:g.139581531_139581535dup , CM000671.1:g.139581531_139581535dup GRCh37
NC_000009.10:g.138701352_138701356dup NCBI36
NG_008090.1:g.5381_5385dup

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.182+97_182+101dup MANE Select ENSP00000360761.2:n.182+97_182+101dup
ENST00000371694.7:c.182+97_182+101dup ENSP00000360759.3:n.182+97_182+101dup
ENST00000371696.6:c.182+97_182+101dup ENSP00000360761.2:n.182+97_182+101dup
ENST00000470861.1:n.190+97_190+101dup
ENST00000538402.1:c.182+97_182+101dup ENSP00000438919.1:n.182+97_182+101dup
NM_001012727.1:c.182+97_182+101dup NP_001012745.1:n.182+97_182+101dup
NM_006412.3:c.182+97_182+101dup NP_006403.2:n.182+97_182+101dup
NM_006412.4:c.182+97_182+101dup MANE Select NP_006403.2:n.182+97_182+101dup
NM_001012727.2:c.182+97_182+101dup NP_001012745.1:n.182+97_182+101dup
Search 100 bp 5'
Search 100 bp 3'