Canonical Allele Identifier: CA861089685
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1359963340
MyVariant Identifiers: chr9:g.139581784_139581785insCGGCCAGACA (hg19) chr9:g.136687332_136687333insCGGCCAGACA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687339_136687348dup , CM000671.2:g.136687339_136687348dup GRCh38
NC_000009.11:g.139581791_139581800dup , CM000671.1:g.139581791_139581800dup GRCh37
NC_000009.10:g.138701612_138701621dup NCBI36
NG_008090.1:g.5118_5127dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.16_25dup MANE Select ENSP00000360761.2:p.Ala9ValfsTer?
ENST00000371694.7:c.16_25dup ENSP00000360759.3:p.Ala9ValfsTer?
ENST00000371696.6:c.16_25dup ENSP00000360761.2:p.Ala9ValfsTer?
ENST00000470861.1:n.24_33dup
ENST00000538402.1:c.16_25dup ENSP00000438919.1:p.Ala9ValfsTer?
NM_001012727.1:c.16_25dup NP_001012745.1:p.Ala9ValfsTer?
NM_006412.3:c.16_25dup NP_006403.2:p.Ala9ValfsTer?
NM_006412.4:c.16_25dup MANE Select NP_006403.2:p.Ala9ValfsTer?
NM_001012727.2:c.16_25dup NP_001012745.1:p.Ala9ValfsTer?
Search 100 bp 5'
Search 100 bp 3'