Canonical Allele Identifier: CA375581040
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136676625G>C , CM000671.2:g.136676625G>C GRCh38
NC_000009.11:g.139571077G>C , CM000671.1:g.139571077G>C GRCh37
NC_000009.10:g.138690898G>C NCBI36
NG_008090.1:g.15835C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.548C>G MANE Select ENSP00000360761.2:p.Pro183Arg
ENST00000371694.7:c.492+336C>G ENSP00000360759.3:n.492+336C>G
ENST00000371696.6:c.548C>G ENSP00000360761.2:p.Pro183Arg
ENST00000472820.1:n.476C>G
ENST00000538402.1:c.548C>G ENSP00000438919.1:p.Pro183Arg
NM_001012727.1:c.492+336C>G NP_001012745.1:n.492+336C>G
NM_006412.3:c.548C>G NP_006403.2:p.Pro183Arg
NM_006412.4:c.548C>G MANE Select NP_006403.2:p.Pro183Arg
NM_001012727.2:c.492+336C>G NP_001012745.1:n.492+336C>G