Canonical Allele Identifier: CA2746816769

Gene: SOAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179354302_179354303insGCC , CM000663.2:g.179354302_179354303insGCC	GRCh38
NC_000001.10:g.179323437_179323438insGCC , CM000663.1:g.179323437_179323438insGCC	GRCh37
NC_000001.9:g.177590060_177590061insGCC	NCBI36
NG_030638.1:g.65589_65590insGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367619.8:c.*661_*662insGCC MANE Select	ENSP00000356591.3:n.*661_*662insGCC
ENST00000367619.7:c.*661_*662insGCC	ENSP00000356591.3:n.*661_*662insGCC
ENST00000539888.5:c.*661_*662insGCC	ENSP00000441356.1:n.*661_*662insGCC
ENST00000540564.5:c.*661_*662insGCC	ENSP00000445315.1:n.*661_*662insGCC
NM_001252511.1:c.*661_*662insGCC	NP_001239440.1:n.*661_*662insGCC
NM_001252512.1:c.*661_*662insGCC	NP_001239441.1:n.*661_*662insGCC
NM_003101.5:c.*661_*662insGCC	NP_003092.4:n.*661_*662insGCC
NR_045530.1:n.2464_2465insGCC
XM_011509911.1:c.*661_*662insGCC	XP_011508213.1:n.*661_*662insGCC
NM_003101.6:c.*661_*662insGCC MANE Select	NP_003092.4:n.*661_*662insGCC
NR_045530.2:n.2381_2382insGCC
NM_001252511.2:c.*661_*662insGCC	NP_001239440.1:n.*661_*662insGCC
NM_001252512.2:c.*661_*662insGCC	NP_001239441.1:n.*661_*662insGCC