Canonical Allele Identifier: CA2021454363
Gene: ST8SIA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.22212947A= , CM000674.2:g.22212947A= GRCh38
NC_000012.11:g.22365881A= , CM000674.1:g.22365881A= GRCh37
NC_000012.10:g.22257148A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000396037.9:c.585-10909T= MANE Select ENSP00000379353.3:n.585-10909T=
ENST00000261197.7:c.*67-10909T= ENSP00000261197.3:n.*67-10909T=
ENST00000396037.8:c.585-10909T= ENSP00000379353.3:n.585-10909T=
ENST00000508924.2:n.188-10909T=
ENST00000540824.5:c.438-10909T= ENSP00000441707.1:n.438-10909T=
ENST00000544732.5:n.151+36059T=
ENST00000545494.5:n.306-10909T=
ENST00000545524.5:n.249+36059T=
NM_001304450.1:c.156-10909T= NP_001291379.1:n.156-10909T=
NM_003034.3:c.585-10909T= NP_003025.1:n.585-10909T=
XR_931322.1:n.1041+36059T=
NM_001304450.2:c.156-10909T= NP_001291379.1:n.156-10909T=
NM_003034.4:c.585-10909T= MANE Select NP_003025.1:n.585-10909T=