Canonical Allele Identifier: CA1210236592
Gene: SOAT1 HGNC NCBI

Linked Data

dbSNP Id: rs1666838117

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.179354201del , CM000663.2:g.179354201del GRCh38
NC_000001.10:g.179323336del , CM000663.1:g.179323336del GRCh37
NC_000001.9:g.177589959del NCBI36
NG_030638.1:g.65488del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367619.8:c.*560del MANE Select ENSP00000356591.3:n.*560del
ENST00000367619.7:c.*560del ENSP00000356591.3:n.*560del
ENST00000539888.5:c.*560del ENSP00000441356.1:n.*560del
ENST00000540564.5:c.*560del ENSP00000445315.1:n.*560del
NM_001252511.1:c.*560del NP_001239440.1:n.*560del
NM_001252512.1:c.*560del NP_001239441.1:n.*560del
NM_003101.5:c.*560del NP_003092.4:n.*560del
NR_045530.1:n.2363del
XM_011509911.1:c.*560del XP_011508213.1:n.*560del
NM_003101.6:c.*560del MANE Select NP_003092.4:n.*560del
NR_045530.2:n.2280del
NM_001252511.2:c.*560del NP_001239440.1:n.*560del
NM_001252512.2:c.*560del NP_001239441.1:n.*560del