Canonical Allele Identifier: CA375577238
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.767T>G MANE Select ENSP00000360761.2:p.Phe256Cys
ENST00000371694.7:c.671T>G ENSP00000360759.3:p.Phe224Cys
ENST00000371696.6:c.767T>G ENSP00000360761.2:p.Phe256Cys
ENST00000472820.1:n.695T>G
ENST00000538402.1:c.767T>G ENSP00000438919.1:p.Phe256Cys
NM_001012727.1:c.671T>G NP_001012745.1:p.Phe224Cys
NM_006412.3:c.767T>G NP_006403.2:p.Phe256Cys
NM_006412.4:c.767T>G MANE Select NP_006403.2:p.Phe256Cys
NM_001012727.2:c.671T>G NP_001012745.1:p.Phe224Cys