Canonical Allele Identifier: CA375577235
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673821G>C , CM000671.2:g.136673821G>C GRCh38
NC_000009.11:g.139568273G>C , CM000671.1:g.139568273G>C GRCh37
NC_000009.10:g.138688094G>C NCBI36
NG_008090.1:g.18639C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.768C>G MANE Select ENSP00000360761.2:p.Phe256Leu
ENST00000371694.7:c.672C>G ENSP00000360759.3:p.Phe224Leu
ENST00000371696.6:c.768C>G ENSP00000360761.2:p.Phe256Leu
ENST00000472820.1:n.696C>G
ENST00000538402.1:c.768C>G ENSP00000438919.1:p.Phe256Leu
NM_001012727.1:c.672C>G NP_001012745.1:p.Phe224Leu
NM_006412.3:c.768C>G NP_006403.2:p.Phe256Leu
NM_006412.4:c.768C>G MANE Select NP_006403.2:p.Phe256Leu
NM_001012727.2:c.672C>G NP_001012745.1:p.Phe224Leu