Canonical Allele Identifier: CA2580617654
Gene: AGPAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674749T= , CM000671.2:g.136674749T= GRCh38
NC_000009.11:g.139569201T= , CM000671.1:g.139569201T= GRCh37
NC_000009.10:g.138689022T= NCBI36
NG_008090.1:g.17711A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.647A= MANE Select ENSP00000360761.2:p.Lys216=
ENST00000371694.7:c.551A= ENSP00000360759.3:p.Lys184=
ENST00000371696.6:c.647A= ENSP00000360761.2:p.Lys216=
ENST00000472820.1:n.575A=
ENST00000538402.1:c.647A= ENSP00000438919.1:p.Lys216=
NM_001012727.1:c.551A= NP_001012745.1:p.Lys184=
NM_006412.3:c.647A= NP_006403.2:p.Lys216=
NM_006412.4:c.647A= MANE Select NP_006403.2:p.Lys216=
NM_001012727.2:c.551A= NP_001012745.1:p.Lys184=