Canonical Allele Identifier: CA5343163
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs770064292

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687210G>A , CM000671.2:g.136687210G>A GRCh38
NC_000009.11:g.139581662G>A , CM000671.1:g.139581662G>A GRCh37
NC_000009.10:g.138701483G>A NCBI36
NG_008090.1:g.5250C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.148C>T MANE Select ENSP00000360761.2:p.Leu50=
ENST00000371694.7:c.148C>T ENSP00000360759.3:p.Leu50=
ENST00000371696.6:c.148C>T ENSP00000360761.2:p.Leu50=
ENST00000470861.1:n.156C>T
ENST00000538402.1:c.148C>T ENSP00000438919.1:p.Leu50=
NM_001012727.1:c.148C>T NP_001012745.1:p.Leu50=
NM_006412.3:c.148C>T NP_006403.2:p.Leu50=
NM_006412.4:c.148C>T MANE Select NP_006403.2:p.Leu50=
NM_001012727.2:c.148C>T NP_001012745.1:p.Leu50=