Canonical Allele Identifier: CA375581051
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136676626G>C , CM000671.2:g.136676626G>C GRCh38
NC_000009.11:g.139571078G>C , CM000671.1:g.139571078G>C GRCh37
NC_000009.10:g.138690899G>C NCBI36
NG_008090.1:g.15834C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.547C>G MANE Select ENSP00000360761.2:p.Pro183Ala
ENST00000371694.7:c.492+335C>G ENSP00000360759.3:n.492+335C>G
ENST00000371696.6:c.547C>G ENSP00000360761.2:p.Pro183Ala
ENST00000472820.1:n.475C>G
ENST00000538402.1:c.547C>G ENSP00000438919.1:p.Pro183Ala
NM_001012727.1:c.492+335C>G NP_001012745.1:n.492+335C>G
NM_006412.3:c.547C>G NP_006403.2:p.Pro183Ala
NM_006412.4:c.547C>G MANE Select NP_006403.2:p.Pro183Ala
NM_001012727.2:c.492+335C>G NP_001012745.1:n.492+335C>G