Canonical Allele Identifier: CA2579519863
Gene: AGPAT2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673652_136673674del , CM000671.2:g.136673652_136673674del GRCh38
NC_000009.11:g.139568104_139568126del , CM000671.1:g.139568104_139568126del GRCh37
NC_000009.10:g.138687925_138687947del NCBI36
NG_008090.1:g.18792_18814del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.*84_*106del MANE Select ENSP00000360761.2:n.*84_*106del
ENST00000371694.7:c.*84_*106del ENSP00000360759.3:n.*84_*106del
ENST00000371696.6:c.*84_*106del ENSP00000360761.2:n.*84_*106del
ENST00000538402.1:c.*84_*106del ENSP00000438919.1:n.*84_*106del
NM_001012727.1:c.*84_*106del NP_001012745.1:n.*84_*106del
NM_006412.3:c.*84_*106del NP_006403.2:n.*84_*106del
NM_006412.4:c.*84_*106del MANE Select NP_006403.2:n.*84_*106del
NM_001012727.2:c.*84_*106del NP_001012745.1:n.*84_*106del
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