Canonical Allele Identifier: CA5343207
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs376582855
ExAC: 9:139581842 TCGCTCCCGCTCC / T
gnomAD v2: 9-139581842-TCGCTCCCGCTCC-T
gnomAD v3: 9-136687390-TCGCTCCCGCTCC-T
gnomAD v4: 9-136687390-TCGCTCCCGCTCC-T
MyVariant Identifiers: chr9:g.139581843_139581854del (hg19) chr9:g.136687391_136687402del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687401_136687412del , CM000671.2:g.136687401_136687412del GRCh38
NC_000009.11:g.139581853_139581864del , CM000671.1:g.139581853_139581864del GRCh37
NC_000009.10:g.138701674_138701685del NCBI36
NG_008090.1:g.5058_5069del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.-45_-34del MANE Select ENSP00000360761.2:n.-45_-34del
ENST00000371696.6:c.-45_-34del ENSP00000360761.2:n.-45_-34del
NM_001012727.1:c.-45_-34del NP_001012745.1:n.-45_-34del
NM_006412.3:c.-45_-34del NP_006403.2:n.-45_-34del
NM_006412.4:c.-45_-34del MANE Select NP_006403.2:n.-45_-34del
NM_001012727.2:c.-45_-34del NP_001012745.1:n.-45_-34del
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