Canonical Allele Identifier: CA1210236595
Gene: SOAT1 HGNC NCBI

Linked Data

dbSNP Id: rs1666838259

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.179354209G>T , CM000663.2:g.179354209G>T GRCh38
NC_000001.10:g.179323344G>T , CM000663.1:g.179323344G>T GRCh37
NC_000001.9:g.177589967G>T NCBI36
NG_030638.1:g.65496G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367619.8:c.*568G>T MANE Select ENSP00000356591.3:n.*568G>T
ENST00000367619.7:c.*568G>T ENSP00000356591.3:n.*568G>T
ENST00000539888.5:c.*568G>T ENSP00000441356.1:n.*568G>T
ENST00000540564.5:c.*568G>T ENSP00000445315.1:n.*568G>T
NM_001252511.1:c.*568G>T NP_001239440.1:n.*568G>T
NM_001252512.1:c.*568G>T NP_001239441.1:n.*568G>T
NM_003101.5:c.*568G>T NP_003092.4:n.*568G>T
NR_045530.1:n.2371G>T
XM_011509911.1:c.*568G>T XP_011508213.1:n.*568G>T
NM_003101.6:c.*568G>T MANE Select NP_003092.4:n.*568G>T
NR_045530.2:n.2288G>T
NM_001252511.2:c.*568G>T NP_001239440.1:n.*568G>T
NM_001252512.2:c.*568G>T NP_001239441.1:n.*568G>T