Canonical Allele Identifier: CA2573612990
Gene: SOAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.179354252T>A , CM000663.2:g.179354252T>A GRCh38
NC_000001.10:g.179323387T>A , CM000663.1:g.179323387T>A GRCh37
NC_000001.9:g.177590010T>A NCBI36
NG_030638.1:g.65539T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367619.8:c.*611T>A MANE Select ENSP00000356591.3:n.*611T>A
ENST00000367619.7:c.*611T>A ENSP00000356591.3:n.*611T>A
ENST00000539888.5:c.*611T>A ENSP00000441356.1:n.*611T>A
ENST00000540564.5:c.*611T>A ENSP00000445315.1:n.*611T>A
NM_001252511.1:c.*611T>A NP_001239440.1:n.*611T>A
NM_001252512.1:c.*611T>A NP_001239441.1:n.*611T>A
NM_003101.5:c.*611T>A NP_003092.4:n.*611T>A
NR_045530.1:n.2414T>A
XM_011509911.1:c.*611T>A XP_011508213.1:n.*611T>A
NM_003101.6:c.*611T>A MANE Select NP_003092.4:n.*611T>A
NR_045530.2:n.2331T>A
NM_001252511.2:c.*611T>A NP_001239440.1:n.*611T>A
NM_001252512.2:c.*611T>A NP_001239441.1:n.*611T>A