Canonical Allele Identifier: CA2692654246
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674818G>A , CM000671.2:g.136674818G>A GRCh38
NC_000009.11:g.139569270G>A , CM000671.1:g.139569270G>A GRCh37
NC_000009.10:g.138689091G>A NCBI36
NG_008090.1:g.17642C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.589-11C>T MANE Select ENSP00000360761.2:n.589-11C>T
ENST00000371694.7:c.493-11C>T ENSP00000360759.3:n.493-11C>T
ENST00000371696.6:c.589-11C>T ENSP00000360761.2:n.589-11C>T
ENST00000472820.1:n.517-11C>T
ENST00000538402.1:c.589-11C>T ENSP00000438919.1:n.589-11C>T
NM_001012727.1:c.493-11C>T NP_001012745.1:n.493-11C>T
NM_006412.3:c.589-11C>T NP_006403.2:n.589-11C>T
NM_006412.4:c.589-11C>T MANE Select NP_006403.2:n.589-11C>T
NM_001012727.2:c.493-11C>T NP_001012745.1:n.493-11C>T