Canonical Allele Identifier: CA2021454283
Gene: ST8SIA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.22212832_22212836delinsATAGT , CM000674.2:g.22212832_22212836delinsATAGT GRCh38
NC_000012.11:g.22365766_22365770delinsATAGT , CM000674.1:g.22365766_22365770delinsATAGT GRCh37
NC_000012.10:g.22257033_22257037delinsATAGT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000396037.9:c.585-10798_585-10794delinsACTAT MANE Select ENSP00000379353.3:n.585-10798_585-10794delinsACTAT
ENST00000261197.7:c.*67-10798_*67-10794delinsACTAT ENSP00000261197.3:n.*67-10798_*67-10794delinsACTAT
ENST00000396037.8:c.585-10798_585-10794delinsACTAT ENSP00000379353.3:n.585-10798_585-10794delinsACTAT
ENST00000508924.2:n.188-10798_188-10794delinsACTAT
ENST00000540824.5:c.438-10798_438-10794delinsACTAT ENSP00000441707.1:n.438-10798_438-10794delinsACTAT
ENST00000544732.5:n.151+36170_151+36174delinsACTAT
ENST00000545494.5:n.306-10798_306-10794delinsACTAT
ENST00000545524.5:n.249+36170_249+36174delinsACTAT
NM_001304450.1:c.156-10798_156-10794delinsACTAT NP_001291379.1:n.156-10798_156-10794delinsACTAT
NM_003034.3:c.585-10798_585-10794delinsACTAT NP_003025.1:n.585-10798_585-10794delinsACTAT
XR_931322.1:n.1041+36170_1041+36174delinsACTAT
NM_001304450.2:c.156-10798_156-10794delinsACTAT NP_001291379.1:n.156-10798_156-10794delinsACTAT
NM_003034.4:c.585-10798_585-10794delinsACTAT MANE Select NP_003025.1:n.585-10798_585-10794delinsACTAT