Canonical Allele Identifier: CA1009659563
Gene: SOAT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.179354339_179354340insTAGGAAGTAGGAAGTAGG , CM000663.2:g.179354339_179354340insTAGGAAGTAGGAAGTAGG GRCh38
NC_000001.10:g.179323474_179323475insTAGGAAGTAGGAAGTAGG , CM000663.1:g.179323474_179323475insTAGGAAGTAGGAAGTAGG GRCh37
NC_000001.9:g.177590097_177590098insTAGGAAGTAGGAAGTAGG NCBI36
NG_030638.1:g.65626_65627insTAGGAAGTAGGAAGTAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000367619.8:c.*698_*699insTAGGAAGTAGGAAGTAGG MANE Select ENSP00000356591.3:n.*698_*699insTAGGAAGTAGGAAGTAGG
ENST00000367619.7:c.*698_*699insTAGGAAGTAGGAAGTAGG ENSP00000356591.3:n.*698_*699insTAGGAAGTAGGAAGTAGG
ENST00000539888.5:c.*698_*699insTAGGAAGTAGGAAGTAGG ENSP00000441356.1:n.*698_*699insTAGGAAGTAGGAAGTAGG
ENST00000540564.5:c.*698_*699insTAGGAAGTAGGAAGTAGG ENSP00000445315.1:n.*698_*699insTAGGAAGTAGGAAGTAGG
NM_001252511.1:c.*698_*699insTAGGAAGTAGGAAGTAGG NP_001239440.1:n.*698_*699insTAGGAAGTAGGAAGTAGG
NM_001252512.1:c.*698_*699insTAGGAAGTAGGAAGTAGG NP_001239441.1:n.*698_*699insTAGGAAGTAGGAAGTAGG
NM_003101.5:c.*698_*699insTAGGAAGTAGGAAGTAGG NP_003092.4:n.*698_*699insTAGGAAGTAGGAAGTAGG
NR_045530.1:n.2501_2502insTAGGAAGTAGGAAGTAGG
XM_011509911.1:c.*698_*699insTAGGAAGTAGGAAGTAGG XP_011508213.1:n.*698_*699insTAGGAAGTAGGAAGTAGG
NM_003101.6:c.*698_*699insTAGGAAGTAGGAAGTAGG MANE Select NP_003092.4:n.*698_*699insTAGGAAGTAGGAAGTAGG
NR_045530.2:n.2418_2419insTAGGAAGTAGGAAGTAGG
NM_001252511.2:c.*698_*699insTAGGAAGTAGGAAGTAGG NP_001239440.1:n.*698_*699insTAGGAAGTAGGAAGTAGG
NM_001252512.2:c.*698_*699insTAGGAAGTAGGAAGTAGG NP_001239441.1:n.*698_*699insTAGGAAGTAGGAAGTAGG