Canonical Allele Identifier: CA2786279582
Gene: AGPAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673517_136673525del , CM000671.2:g.136673517_136673525del GRCh38
NC_000009.11:g.139567969_139567977del , CM000671.1:g.139567969_139567977del GRCh37
NC_000009.10:g.138687790_138687798del NCBI36
NG_008090.1:g.18935_18943del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.*227_*235del MANE Select ENSP00000360761.2:n.*227_*235del
ENST00000371694.7:c.*227_*235del ENSP00000360759.3:n.*227_*235del
ENST00000371696.6:c.*227_*235del ENSP00000360761.2:n.*227_*235del
ENST00000538402.1:c.*227_*235del ENSP00000438919.1:n.*227_*235del
NM_001012727.1:c.*227_*235del NP_001012745.1:n.*227_*235del
NM_006412.3:c.*227_*235del NP_006403.2:n.*227_*235del
NM_006412.4:c.*227_*235del MANE Select NP_006403.2:n.*227_*235del
NM_001012727.2:c.*227_*235del NP_001012745.1:n.*227_*235del