Canonical Allele Identifier: CA891805048

Gene: SOAT1

Linked Data

• dbSNP Id: rs1490156713
• MyVariant Identifiers: chr1:g.179323473A>G (hg19) ; chr1:g.179354338A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179354338A>G , CM000663.2:g.179354338A>G	GRCh38
NC_000001.10:g.179323473A>G , CM000663.1:g.179323473A>G	GRCh37
NC_000001.9:g.177590096A>G	NCBI36
NG_030638.1:g.65625A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367619.8:c.*697A>G MANE Select	ENSP00000356591.3:n.*697A>G
ENST00000367619.7:c.*697A>G	ENSP00000356591.3:n.*697A>G
ENST00000539888.5:c.*697A>G	ENSP00000441356.1:n.*697A>G
ENST00000540564.5:c.*697A>G	ENSP00000445315.1:n.*697A>G
NM_001252511.1:c.*697A>G	NP_001239440.1:n.*697A>G
NM_001252512.1:c.*697A>G	NP_001239441.1:n.*697A>G
NM_003101.5:c.*697A>G	NP_003092.4:n.*697A>G
NR_045530.1:n.2500A>G
XM_011509911.1:c.*697A>G	XP_011508213.1:n.*697A>G
NM_003101.6:c.*697A>G MANE Select	NP_003092.4:n.*697A>G
NR_045530.2:n.2417A>G
NM_001252511.2:c.*697A>G	NP_001239440.1:n.*697A>G
NM_001252512.2:c.*697A>G	NP_001239441.1:n.*697A>G