Canonical Allele Identifier: CA375578320
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674752T>G , CM000671.2:g.136674752T>G GRCh38
NC_000009.11:g.139569204T>G , CM000671.1:g.139569204T>G GRCh37
NC_000009.10:g.138689025T>G NCBI36
NG_008090.1:g.17708A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.644A>C MANE Select ENSP00000360761.2:p.Lys215Thr
ENST00000371694.7:c.548A>C ENSP00000360759.3:p.Lys183Thr
ENST00000371696.6:c.644A>C ENSP00000360761.2:p.Lys215Thr
ENST00000472820.1:n.572A>C
ENST00000538402.1:c.644A>C ENSP00000438919.1:p.Lys215Thr
NM_001012727.1:c.548A>C NP_001012745.1:p.Lys183Thr
NM_006412.3:c.644A>C NP_006403.2:p.Lys215Thr
NM_006412.4:c.644A>C MANE Select NP_006403.2:p.Lys215Thr
NM_001012727.2:c.548A>C NP_001012745.1:p.Lys183Thr