Canonical Allele Identifier: CA2695201893
Gene: AGPAT2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673534T= , CM000671.2:g.136673534T= GRCh38
NC_000009.11:g.139567986T= , CM000671.1:g.139567986T= GRCh37
NC_000009.10:g.138687807T= NCBI36
NG_008090.1:g.18926A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.*218A= MANE Select ENSP00000360761.2:n.*218A=
ENST00000371694.7:c.*218A= ENSP00000360759.3:n.*218A=
ENST00000371696.6:c.*218A= ENSP00000360761.2:n.*218A=
ENST00000538402.1:c.*218A= ENSP00000438919.1:n.*218A=
NM_001012727.1:c.*218A= NP_001012745.1:n.*218A=
NM_006412.3:c.*218A= NP_006403.2:n.*218A=
NM_006412.4:c.*218A= MANE Select NP_006403.2:n.*218A=
NM_001012727.2:c.*218A= NP_001012745.1:n.*218A=
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