Canonical Allele Identifier: CA1210236606

Gene: SOAT1

Linked Data

• dbSNP Id: rs1666838984

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179354232T>A , CM000663.2:g.179354232T>A	GRCh38
NC_000001.10:g.179323367T>A , CM000663.1:g.179323367T>A	GRCh37
NC_000001.9:g.177589990T>A	NCBI36
NG_030638.1:g.65519T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367619.8:c.*591T>A MANE Select	ENSP00000356591.3:n.*591T>A
ENST00000367619.7:c.*591T>A	ENSP00000356591.3:n.*591T>A
ENST00000539888.5:c.*591T>A	ENSP00000441356.1:n.*591T>A
ENST00000540564.5:c.*591T>A	ENSP00000445315.1:n.*591T>A
NM_001252511.1:c.*591T>A	NP_001239440.1:n.*591T>A
NM_001252512.1:c.*591T>A	NP_001239441.1:n.*591T>A
NM_003101.5:c.*591T>A	NP_003092.4:n.*591T>A
NR_045530.1:n.2394T>A
XM_011509911.1:c.*591T>A	XP_011508213.1:n.*591T>A
NM_003101.6:c.*591T>A MANE Select	NP_003092.4:n.*591T>A
NR_045530.2:n.2311T>A
NM_001252511.2:c.*591T>A	NP_001239440.1:n.*591T>A
NM_001252512.2:c.*591T>A	NP_001239441.1:n.*591T>A