Canonical Allele Identifier: CA375581128
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136676640T>A , CM000671.2:g.136676640T>A GRCh38
NC_000009.11:g.139571092T>A , CM000671.1:g.139571092T>A GRCh37
NC_000009.10:g.138690913T>A NCBI36
NG_008090.1:g.15820A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.533A>T MANE Select ENSP00000360761.2:p.Asn178Ile
ENST00000371694.7:c.492+321A>T ENSP00000360759.3:n.492+321A>T
ENST00000371696.6:c.533A>T ENSP00000360761.2:p.Asn178Ile
ENST00000472820.1:n.461A>T
ENST00000538402.1:c.533A>T ENSP00000438919.1:p.Asn178Ile
NM_001012727.1:c.492+321A>T NP_001012745.1:n.492+321A>T
NM_006412.3:c.533A>T NP_006403.2:p.Asn178Ile
NM_006412.4:c.533A>T MANE Select NP_006403.2:p.Asn178Ile
NM_001012727.2:c.492+321A>T NP_001012745.1:n.492+321A>T