Canonical Allele Identifier: CA1130033698
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674703_136674714del , CM000671.2:g.136674703_136674714del GRCh38
NC_000009.11:g.139569155_139569166del , CM000671.1:g.139569155_139569166del GRCh37
NC_000009.10:g.138688976_138688987del NCBI36
NG_008090.1:g.17748_17759del

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.661+23_661+34del MANE Select ENSP00000360761.2:n.661+23_661+34del
ENST00000371694.7:c.565+23_565+34del ENSP00000360759.3:n.565+23_565+34del
ENST00000371696.6:c.661+23_661+34del ENSP00000360761.2:n.661+23_661+34del
ENST00000472820.1:n.589+23_589+34del
ENST00000538402.1:c.661+23_661+34del ENSP00000438919.1:n.661+23_661+34del
NM_001012727.1:c.565+23_565+34del NP_001012745.1:n.565+23_565+34del
NM_006412.3:c.661+23_661+34del NP_006403.2:n.661+23_661+34del
NM_006412.4:c.661+23_661+34del MANE Select NP_006403.2:n.661+23_661+34del
NM_001012727.2:c.565+23_565+34del NP_001012745.1:n.565+23_565+34del