Canonical Allele Identifier: CA201641597
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs376582855
gnomAD v2: 9-139581842-T-TCGCTCC
gnomAD v3: 9-136687390-T-TCGCTCC
gnomAD v4: 9-136687390-T-TCGCTCC
MyVariant Identifiers: chr9:g.139581854_139581855insCGCTCC (hg19) chr9:g.139581842_139581843insCGCTCC (hg19) chr9:g.136687402_136687403insCGCTCC (hg38) chr9:g.136687390_136687391insCGCTCC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687407_136687412dup , CM000671.2:g.136687407_136687412dup GRCh38
NC_000009.11:g.139581859_139581864dup , CM000671.1:g.139581859_139581864dup GRCh37
NC_000009.10:g.138701680_138701685dup NCBI36
NG_008090.1:g.5064_5069dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.-39_-34dup MANE Select ENSP00000360761.2:n.-39_-34dup
ENST00000371696.6:c.-39_-34dup ENSP00000360761.2:n.-39_-34dup
NM_001012727.1:c.-39_-34dup NP_001012745.1:n.-39_-34dup
NM_006412.3:c.-39_-34dup NP_006403.2:n.-39_-34dup
NM_006412.4:c.-39_-34dup MANE Select NP_006403.2:n.-39_-34dup
NM_001012727.2:c.-39_-34dup NP_001012745.1:n.-39_-34dup
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Search 100 bp 3'