Canonical Allele Identifier: CA2720874574
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs2119180045
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674733dup , CM000671.2:g.136674733dup GRCh38
NC_000009.11:g.139569185dup , CM000671.1:g.139569185dup GRCh37
NC_000009.10:g.138689006dup NCBI36
NG_008090.1:g.17727dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.661+2dup MANE Select ENSP00000360761.2:n.661+2dup
ENST00000371694.7:c.565+2dup ENSP00000360759.3:n.565+2dup
ENST00000371696.6:c.661+2dup ENSP00000360761.2:n.661+2dup
ENST00000472820.1:n.589+2dup
ENST00000538402.1:c.661+2dup ENSP00000438919.1:n.661+2dup
NM_001012727.1:c.565+2dup NP_001012745.1:n.565+2dup
NM_006412.3:c.661+2dup NP_006403.2:n.661+2dup
NM_006412.4:c.661+2dup MANE Select NP_006403.2:n.661+2dup
NM_001012727.2:c.565+2dup NP_001012745.1:n.565+2dup
Search 100 bp 5'
Search 100 bp 3'