Canonical Allele Identifier: CA375587816
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687176C>G , CM000671.2:g.136687176C>G GRCh38
NC_000009.11:g.139581628C>G , CM000671.1:g.139581628C>G GRCh37
NC_000009.10:g.138701449C>G NCBI36
NG_008090.1:g.5284G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.182G>C MANE Select ENSP00000360761.2:p.Ser61Thr
ENST00000371694.7:c.182G>C ENSP00000360759.3:p.Ser61Thr
ENST00000371696.6:c.182G>C ENSP00000360761.2:p.Ser61Thr
ENST00000470861.1:n.190G>C
ENST00000538402.1:c.182G>C ENSP00000438919.1:p.Ser61Thr
NM_001012727.1:c.182G>C NP_001012745.1:p.Ser61Thr
NM_006412.3:c.182G>C NP_006403.2:p.Ser61Thr
NM_006412.4:c.182G>C MANE Select NP_006403.2:p.Ser61Thr
NM_001012727.2:c.182G>C NP_001012745.1:p.Ser61Thr