Canonical Allele Identifier: CA2649304923
Gene: SOAT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.179354344del , CM000663.2:g.179354344del GRCh38
NC_000001.10:g.179323479del , CM000663.1:g.179323479del GRCh37
NC_000001.9:g.177590102del NCBI36
NG_030638.1:g.65631del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367619.8:c.*703del MANE Select ENSP00000356591.3:n.*703del
ENST00000367619.7:c.*703del ENSP00000356591.3:n.*703del
ENST00000539888.5:c.*703del ENSP00000441356.1:n.*703del
ENST00000540564.5:c.*703del ENSP00000445315.1:n.*703del
NM_001252511.1:c.*703del NP_001239440.1:n.*703del
NM_001252512.1:c.*703del NP_001239441.1:n.*703del
NM_003101.5:c.*703del NP_003092.4:n.*703del
NR_045530.1:n.2506del
XM_011509911.1:c.*703del XP_011508213.1:n.*703del
NM_003101.6:c.*703del MANE Select NP_003092.4:n.*703del
NR_045530.2:n.2423del
NM_001252511.2:c.*703del NP_001239440.1:n.*703del
NM_001252512.2:c.*703del NP_001239441.1:n.*703del