Canonical Allele Identifier: CA5342882
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs777462050

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674718_136674725del , CM000671.2:g.136674718_136674725del GRCh38
NC_000009.11:g.139569170_139569177del , CM000671.1:g.139569170_139569177del GRCh37
NC_000009.10:g.138688991_138688998del NCBI36
NG_008090.1:g.17737_17744del

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.661+12_661+19del MANE Select ENSP00000360761.2:n.661+12_661+19del
ENST00000371694.7:c.565+12_565+19del ENSP00000360759.3:n.565+12_565+19del
ENST00000371696.6:c.661+12_661+19del ENSP00000360761.2:n.661+12_661+19del
ENST00000472820.1:n.589+12_589+19del
ENST00000538402.1:c.661+12_661+19del ENSP00000438919.1:n.661+12_661+19del
NM_001012727.1:c.565+12_565+19del NP_001012745.1:n.565+12_565+19del
NM_006412.3:c.661+12_661+19del NP_006403.2:n.661+12_661+19del
NM_006412.4:c.661+12_661+19del MANE Select NP_006403.2:n.661+12_661+19del
NM_001012727.2:c.565+12_565+19del NP_001012745.1:n.565+12_565+19del