Canonical Allele Identifier: CA375588217
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687278T>C , CM000671.2:g.136687278T>C GRCh38
NC_000009.11:g.139581730T>C , CM000671.1:g.139581730T>C GRCh37
NC_000009.10:g.138701551T>C NCBI36
NG_008090.1:g.5182A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.80A>G MANE Select ENSP00000360761.2:p.Tyr27Cys
ENST00000371694.7:c.80A>G ENSP00000360759.3:p.Tyr27Cys
ENST00000371696.6:c.80A>G ENSP00000360761.2:p.Tyr27Cys
ENST00000470861.1:n.88A>G
ENST00000538402.1:c.80A>G ENSP00000438919.1:p.Tyr27Cys
NM_001012727.1:c.80A>G NP_001012745.1:p.Tyr27Cys
NM_006412.3:c.80A>G NP_006403.2:p.Tyr27Cys
NM_006412.4:c.80A>G MANE Select NP_006403.2:p.Tyr27Cys
NM_001012727.2:c.80A>G NP_001012745.1:p.Tyr27Cys