Canonical Allele Identifier: CA2021454379
Gene: ST8SIA1 HGNC NCBI

Linked Data

dbSNP Id: rs1865190526

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.22212969_22212970insAG , CM000674.2:g.22212969_22212970insAG GRCh38
NC_000012.11:g.22365903_22365904insAG , CM000674.1:g.22365903_22365904insAG GRCh37
NC_000012.10:g.22257170_22257171insAG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000396037.9:c.585-10932_585-10931insCT MANE Select ENSP00000379353.3:n.585-10932_585-10931in...
ENST00000261197.7:c.*67-10932_*67-10931insCT ENSP00000261197.3:n.*67-10932_*67-10931in...
ENST00000396037.8:c.585-10932_585-10931insCT ENSP00000379353.3:n.585-10932_585-10931in...
ENST00000508924.2:n.188-10932_188-10931insCT
ENST00000540824.5:c.438-10932_438-10931insCT ENSP00000441707.1:n.438-10932_438-10931in...
ENST00000544732.5:n.151+36036_151+36037insCT
ENST00000545494.5:n.306-10932_306-10931insCT
ENST00000545524.5:n.249+36036_249+36037insCT
NM_001304450.1:c.156-10932_156-10931insCT NP_001291379.1:n.156-10932_156-10931insCT...
NM_003034.3:c.585-10932_585-10931insCT NP_003025.1:n.585-10932_585-10931insCT
XR_931322.1:n.1041+36036_1041+36037insCT
NM_001304450.2:c.156-10932_156-10931insCT NP_001291379.1:n.156-10932_156-10931insCT...
NM_003034.4:c.585-10932_585-10931insCT MANE Select NP_003025.1:n.585-10932_585-10931insCT