Canonical Allele Identifier: CA2497275639
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1846231041
gnomAD v4: 9-136687066-G-GGAGCGGGGCGGGAC
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687068_136687081dup , CM000671.2:g.136687068_136687081dup GRCh38
NC_000009.11:g.139581520_139581533dup , CM000671.1:g.139581520_139581533dup GRCh37
NC_000009.10:g.138701341_138701354dup NCBI36
NG_008090.1:g.5380_5393dup

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.182+96_182+109dup MANE Select ENSP00000360761.2:n.182+96_182+109dup
ENST00000371694.7:c.182+96_182+109dup ENSP00000360759.3:n.182+96_182+109dup
ENST00000371696.6:c.182+96_182+109dup ENSP00000360761.2:n.182+96_182+109dup
ENST00000470861.1:n.190+96_190+109dup
ENST00000538402.1:c.182+96_182+109dup ENSP00000438919.1:n.182+96_182+109dup
NM_001012727.1:c.182+96_182+109dup NP_001012745.1:n.182+96_182+109dup
NM_006412.3:c.182+96_182+109dup NP_006403.2:n.182+96_182+109dup
NM_006412.4:c.182+96_182+109dup MANE Select NP_006403.2:n.182+96_182+109dup
NM_001012727.2:c.182+96_182+109dup NP_001012745.1:n.182+96_182+109dup
Search 100 bp 5'
Search 100 bp 3'