Canonical Allele Identifier: CA2720909694
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs2131023948
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687320_136687321insTCA , CM000671.2:g.136687320_136687321insTCA GRCh38
NC_000009.11:g.139581772_139581773insTCA , CM000671.1:g.139581772_139581773insTCA GRCh37
NC_000009.10:g.138701593_138701594insTCA NCBI36
NG_008090.1:g.5141_5142insATG

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.39_40insATG MANE Select ENSP00000360761.2:p.Leu13_Leu14insMet
ENST00000371694.7:c.39_40insATG ENSP00000360759.3:p.Leu13_Leu14insMet
ENST00000371696.6:c.39_40insATG ENSP00000360761.2:p.Leu13_Leu14insMet
ENST00000470861.1:n.47_48insATG
ENST00000538402.1:c.39_40insATG ENSP00000438919.1:p.Leu13_Leu14insMet
NM_001012727.1:c.39_40insATG NP_001012745.1:p.Leu13_Leu14insMet
NM_006412.3:c.39_40insATG NP_006403.2:p.Leu13_Leu14insMet
NM_006412.4:c.39_40insATG MANE Select NP_006403.2:p.Leu13_Leu14insMet
NM_001012727.2:c.39_40insATG NP_001012745.1:p.Leu13_Leu14insMet
Search 100 bp 5'
Search 100 bp 3'