Canonical Allele Identifier: CA375576072
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1344825112

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673759G>T , CM000671.2:g.136673759G>T GRCh38
NC_000009.11:g.139568211G>T , CM000671.1:g.139568211G>T GRCh37
NC_000009.10:g.138688032G>T NCBI36
NG_008090.1:g.18701C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.830C>A MANE Select ENSP00000360761.2:p.Ala277Asp
ENST00000371694.7:c.734C>A ENSP00000360759.3:p.Ala245Asp
ENST00000371696.6:c.830C>A ENSP00000360761.2:p.Ala277Asp
ENST00000472820.1:n.758C>A
ENST00000538402.1:c.830C>A ENSP00000438919.1:p.Ala277Asp
NM_001012727.1:c.734C>A NP_001012745.1:p.Ala245Asp
NM_006412.3:c.830C>A NP_006403.2:p.Ala277Asp
NM_006412.4:c.830C>A MANE Select NP_006403.2:p.Ala277Asp
NM_001012727.2:c.734C>A NP_001012745.1:p.Ala245Asp