Canonical Allele Identifier: CA1210236618
Gene: SOAT1 HGNC NCBI

Linked Data

dbSNP Id: rs1666839764

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.179354278dup , CM000663.2:g.179354278dup GRCh38
NC_000001.10:g.179323413dup , CM000663.1:g.179323413dup GRCh37
NC_000001.9:g.177590036dup NCBI36
NG_030638.1:g.65565dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000367619.8:c.*637dup MANE Select ENSP00000356591.3:n.*637dup
ENST00000367619.7:c.*637dup ENSP00000356591.3:n.*637dup
ENST00000539888.5:c.*637dup ENSP00000441356.1:n.*637dup
ENST00000540564.5:c.*637dup ENSP00000445315.1:n.*637dup
NM_001252511.1:c.*637dup NP_001239440.1:n.*637dup
NM_001252512.1:c.*637dup NP_001239441.1:n.*637dup
NM_003101.5:c.*637dup NP_003092.4:n.*637dup
NR_045530.1:n.2440dup
XM_011509911.1:c.*637dup XP_011508213.1:n.*637dup
NM_003101.6:c.*637dup MANE Select NP_003092.4:n.*637dup
NR_045530.2:n.2357dup
NM_001252511.2:c.*637dup NP_001239440.1:n.*637dup
NM_001252512.2:c.*637dup NP_001239441.1:n.*637dup