Canonical Allele Identifier: CA2697519567

Gene: SOAT1

Linked Data

• dbSNP Id: rs1803033

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179354496G>A , CM000663.2:g.179354496G>A	GRCh38
NC_000001.10:g.179323631G>A , CM000663.1:g.179323631G>A	GRCh37
NC_000001.9:g.177590254G>A	NCBI36
NG_030638.1:g.65783G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367619.8:c.*855G>A MANE Select	ENSP00000356591.3:n.*855G>A
ENST00000367619.7:c.*855G>A	ENSP00000356591.3:n.*855G>A
ENST00000539888.5:c.*855G>A	ENSP00000441356.1:n.*855G>A
ENST00000540564.5:c.*855G>A	ENSP00000445315.1:n.*855G>A
NM_001252511.1:c.*855G>A	NP_001239440.1:n.*855G>A
NM_001252512.1:c.*855G>A	NP_001239441.1:n.*855G>A
NM_003101.5:c.*855G>A	NP_003092.4:n.*855G>A
NR_045530.1:n.2658G>A
XM_011509911.1:c.*855G>A	XP_011508213.1:n.*855G>A
NM_003101.6:c.*855G>A MANE Select	NP_003092.4:n.*855G>A
NR_045530.2:n.2575G>A
NM_001252511.2:c.*855G>A	NP_001239440.1:n.*855G>A
NM_001252512.2:c.*855G>A	NP_001239441.1:n.*855G>A