Canonical Allele Identifier: CA2497275505
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1846043453
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673738_136673743del , CM000671.2:g.136673738_136673743del GRCh38
NC_000009.11:g.139568190_139568195del , CM000671.1:g.139568190_139568195del GRCh37
NC_000009.10:g.138688011_138688016del NCBI36
NG_008090.1:g.18717_18722del

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.*9_*14del MANE Select ENSP00000360761.2:n.*9_*14del
ENST00000371694.7:c.*9_*14del ENSP00000360759.3:n.*9_*14del
ENST00000371696.6:c.*9_*14del ENSP00000360761.2:n.*9_*14del
ENST00000472820.1:n.774_779del
ENST00000538402.1:c.*9_*14del ENSP00000438919.1:n.*9_*14del
NM_001012727.1:c.*9_*14del NP_001012745.1:n.*9_*14del
NM_006412.3:c.*9_*14del NP_006403.2:n.*9_*14del
NM_006412.4:c.*9_*14del MANE Select NP_006403.2:n.*9_*14del
NM_001012727.2:c.*9_*14del NP_001012745.1:n.*9_*14del
Search 100 bp 5'
Search 100 bp 3'