Canonical Allele Identifier: CA861081204
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1171305079

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674726_136674728del , CM000671.2:g.136674726_136674728del GRCh38
NC_000009.11:g.139569178_139569180del , CM000671.1:g.139569178_139569180del GRCh37
NC_000009.10:g.138688999_138689001del NCBI36
NG_008090.1:g.17733_17735del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.661+8_661+10del MANE Select ENSP00000360761.2:n.661+8_661+10del
ENST00000371694.7:c.565+8_565+10del ENSP00000360759.3:n.565+8_565+10del
ENST00000371696.6:c.661+8_661+10del ENSP00000360761.2:n.661+8_661+10del
ENST00000472820.1:n.589+8_589+10del
ENST00000538402.1:c.661+8_661+10del ENSP00000438919.1:n.661+8_661+10del
NM_001012727.1:c.565+8_565+10del NP_001012745.1:n.565+8_565+10del
NM_006412.3:c.661+8_661+10del NP_006403.2:n.661+8_661+10del
NM_006412.4:c.661+8_661+10del MANE Select NP_006403.2:n.661+8_661+10del
NM_001012727.2:c.565+8_565+10del NP_001012745.1:n.565+8_565+10del