Canonical Allele Identifier: CA375577240
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673822A>T , CM000671.2:g.136673822A>T GRCh38
NC_000009.11:g.139568274A>T , CM000671.1:g.139568274A>T GRCh37
NC_000009.10:g.138688095A>T NCBI36
NG_008090.1:g.18638T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.767T>A MANE Select ENSP00000360761.2:p.Phe256Tyr
ENST00000371694.7:c.671T>A ENSP00000360759.3:p.Phe224Tyr
ENST00000371696.6:c.767T>A ENSP00000360761.2:p.Phe256Tyr
ENST00000472820.1:n.695T>A
ENST00000538402.1:c.767T>A ENSP00000438919.1:p.Phe256Tyr
NM_001012727.1:c.671T>A NP_001012745.1:p.Phe224Tyr
NM_006412.3:c.767T>A NP_006403.2:p.Phe256Tyr
NM_006412.4:c.767T>A MANE Select NP_006403.2:p.Phe256Tyr
NM_001012727.2:c.671T>A NP_001012745.1:p.Phe224Tyr