Canonical Allele Identifier: CA33643945

Gene: SOAT1

Linked Data

• dbSNP Id: rs908917692
• MyVariant Identifiers: chr1:g.179354512A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179354512A>T , CM000663.2:g.179354512A>T	GRCh38
NC_000001.10:g.179323647A>T , CM000663.1:g.179323647A>T	GRCh37
NC_000001.9:g.177590270A>T	NCBI36
NG_030638.1:g.65799A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367619.8:c.*871A>T MANE Select	ENSP00000356591.3:n.*871A>T
ENST00000367619.7:c.*871A>T	ENSP00000356591.3:n.*871A>T
ENST00000539888.5:c.*871A>T	ENSP00000441356.1:n.*871A>T
ENST00000540564.5:c.*871A>T	ENSP00000445315.1:n.*871A>T
NM_001252511.1:c.*871A>T	NP_001239440.1:n.*871A>T
NM_001252512.1:c.*871A>T	NP_001239441.1:n.*871A>T
NM_003101.5:c.*871A>T	NP_003092.4:n.*871A>T
NR_045530.1:n.2674A>T
XM_011509911.1:c.*871A>T	XP_011508213.1:n.*871A>T
NM_003101.6:c.*871A>T MANE Select	NP_003092.4:n.*871A>T
NR_045530.2:n.2591A>T
NM_001252511.2:c.*871A>T	NP_001239440.1:n.*871A>T
NM_001252512.2:c.*871A>T	NP_001239441.1:n.*871A>T