Canonical Allele Identifier: CA375578539
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674766G>T , CM000671.2:g.136674766G>T GRCh38
NC_000009.11:g.139569218G>T , CM000671.1:g.139569218G>T GRCh37
NC_000009.10:g.138689039G>T NCBI36
NG_008090.1:g.17694C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.630C>A MANE Select ENSP00000360761.2:p.Phe210Leu
ENST00000371694.7:c.534C>A ENSP00000360759.3:p.Phe178Leu
ENST00000371696.6:c.630C>A ENSP00000360761.2:p.Phe210Leu
ENST00000472820.1:n.558C>A
ENST00000538402.1:c.630C>A ENSP00000438919.1:p.Phe210Leu
NM_001012727.1:c.534C>A NP_001012745.1:p.Phe178Leu
NM_006412.3:c.630C>A NP_006403.2:p.Phe210Leu
NM_006412.4:c.630C>A MANE Select NP_006403.2:p.Phe210Leu
NM_001012727.2:c.534C>A NP_001012745.1:p.Phe178Leu