Canonical Allele Identifier: CA375578488
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674763G>C , CM000671.2:g.136674763G>C GRCh38
NC_000009.11:g.139569215G>C , CM000671.1:g.139569215G>C GRCh37
NC_000009.10:g.138689036G>C NCBI36
NG_008090.1:g.17697C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.633C>G MANE Select ENSP00000360761.2:p.Tyr211Ter
ENST00000371694.7:c.537C>G ENSP00000360759.3:p.Tyr179Ter
ENST00000371696.6:c.633C>G ENSP00000360761.2:p.Tyr211Ter
ENST00000472820.1:n.561C>G
ENST00000538402.1:c.633C>G ENSP00000438919.1:p.Tyr211Ter
NM_001012727.1:c.537C>G NP_001012745.1:p.Tyr179Ter
NM_006412.3:c.633C>G NP_006403.2:p.Tyr211Ter
NM_006412.4:c.633C>G MANE Select NP_006403.2:p.Tyr211Ter
NM_001012727.2:c.537C>G NP_001012745.1:p.Tyr179Ter