Canonical Allele Identifier: CA10626924
Gene: AGPAT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 365909
ClinVar RCV Id: RCV000377115 RCV001683449
dbSNP Id: rs145169122
gnomAD v2: 9-139567986-T-TCGAGCC
gnomAD v3: 9-136673534-T-TCGAGCC
gnomAD v4: 9-136673534-T-TCGAGCC
COSMIC: COSN20106744
MyVariant Identifiers: chr9:g.139567987_139567992dupCGAGCC (hg19) chr9:g.139567986_139567987insCGAGCC (hg19) chr9:g.136673535_136673540dupCGAGCC (hg38) chr9:g.136673534_136673535insCGAGCC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673537_136673542dup , CM000671.2:g.136673537_136673542dup GRCh38
NC_000009.11:g.139567989_139567994dup , CM000671.1:g.139567989_139567994dup GRCh37
NC_000009.10:g.138687810_138687815dup NCBI36
NG_008090.1:g.18920_18925dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.*212_*217dup MANE Select ENSP00000360761.2:n.*212_*217dup
ENST00000371694.7:c.*212_*217dup ENSP00000360759.3:n.*212_*217dup
ENST00000371696.6:c.*212_*217dup ENSP00000360761.2:n.*212_*217dup
ENST00000538402.1:c.*212_*217dup ENSP00000438919.1:n.*212_*217dup
NM_001012727.1:c.*212_*217dup NP_001012745.1:n.*212_*217dup
NM_006412.3:c.*212_*217dup NP_006403.2:n.*212_*217dup
NM_006412.4:c.*212_*217dup MANE Select NP_006403.2:n.*212_*217dup
NM_001012727.2:c.*212_*217dup NP_001012745.1:n.*212_*217dup
Search 100 bp 5'
Search 100 bp 3'