Canonical Allele Identifier: CA2692654222
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674767_136674769del , CM000671.2:g.136674767_136674769del GRCh38
NC_000009.11:g.139569219_139569221del , CM000671.1:g.139569219_139569221del GRCh37
NC_000009.10:g.138689040_138689042del NCBI36
NG_008090.1:g.17693_17695del

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.629_631del MANE Select ENSP00000360761.2:p.Phe210del
ENST00000371694.7:c.533_535del ENSP00000360759.3:p.Phe178del
ENST00000371696.6:c.629_631del ENSP00000360761.2:p.Phe210del
ENST00000472820.1:n.557_559del
ENST00000538402.1:c.629_631del ENSP00000438919.1:p.Phe210del
NM_001012727.1:c.533_535del NP_001012745.1:p.Phe178del
NM_006412.3:c.629_631del NP_006403.2:p.Phe210del
NM_006412.4:c.629_631del MANE Select NP_006403.2:p.Phe210del
NM_001012727.2:c.533_535del NP_001012745.1:p.Phe178del