Canonical Allele Identifier: CA1210236698

Gene: SOAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179354484_179354485delinsCT , CM000663.2:g.179354484_179354485delinsCT	GRCh38
NC_000001.10:g.179323619_179323620delinsCT , CM000663.1:g.179323619_179323620delinsCT	GRCh37
NC_000001.9:g.177590242_177590243delinsCT	NCBI36
NG_030638.1:g.65771_65772delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367619.8:c.*843_*844delinsCT MANE Select	ENSP00000356591.3:n.*843_*844delinsCT
ENST00000367619.7:c.*843_*844delinsCT	ENSP00000356591.3:n.*843_*844delinsCT
ENST00000539888.5:c.*843_*844delinsCT	ENSP00000441356.1:n.*843_*844delinsCT
ENST00000540564.5:c.*843_*844delinsCT	ENSP00000445315.1:n.*843_*844delinsCT
NM_001252511.1:c.*843_*844delinsCT	NP_001239440.1:n.*843_*844delinsCT
NM_001252512.1:c.*843_*844delinsCT	NP_001239441.1:n.*843_*844delinsCT
NM_003101.5:c.*843_*844delinsCT	NP_003092.4:n.*843_*844delinsCT
NR_045530.1:n.2646_2647delinsCT
XM_011509911.1:c.*843_*844delinsCT	XP_011508213.1:n.*843_*844delinsCT
NM_003101.6:c.*843_*844delinsCT MANE Select	NP_003092.4:n.*843_*844delinsCT
NR_045530.2:n.2563_2564delinsCT
NM_001252511.2:c.*843_*844delinsCT	NP_001239440.1:n.*843_*844delinsCT
NM_001252512.2:c.*843_*844delinsCT	NP_001239441.1:n.*843_*844delinsCT