Canonical Allele Identifier: CA2692653504
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673587T>A , CM000671.2:g.136673587T>A GRCh38
NC_000009.11:g.139568039T>A , CM000671.1:g.139568039T>A GRCh37
NC_000009.10:g.138687860T>A NCBI36
NG_008090.1:g.18873A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.*165A>T MANE Select ENSP00000360761.2:n.*165A>T
ENST00000371694.7:c.*165A>T ENSP00000360759.3:n.*165A>T
ENST00000371696.6:c.*165A>T ENSP00000360761.2:n.*165A>T
ENST00000538402.1:c.*165A>T ENSP00000438919.1:n.*165A>T
NM_001012727.1:c.*165A>T NP_001012745.1:n.*165A>T
NM_006412.3:c.*165A>T NP_006403.2:n.*165A>T
NM_006412.4:c.*165A>T MANE Select NP_006403.2:n.*165A>T
NM_001012727.2:c.*165A>T NP_001012745.1:n.*165A>T