Canonical Allele Identifier: CA2021454285

Gene: ST8SIA1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.22212833T= , CM000674.2:g.22212833T=	GRCh38
NC_000012.11:g.22365767T= , CM000674.1:g.22365767T=	GRCh37
NC_000012.10:g.22257034T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396037.9:c.585-10795A= MANE Select	ENSP00000379353.3:n.585-10795A=
ENST00000261197.7:c.*67-10795A=	ENSP00000261197.3:n.*67-10795A=
ENST00000396037.8:c.585-10795A=	ENSP00000379353.3:n.585-10795A=
ENST00000508924.2:n.188-10795A=
ENST00000540824.5:c.438-10795A=	ENSP00000441707.1:n.438-10795A=
ENST00000544732.5:n.151+36173A=
ENST00000545494.5:n.306-10795A=
ENST00000545524.5:n.249+36173A=
NM_001304450.1:c.156-10795A=	NP_001291379.1:n.156-10795A=
NM_003034.3:c.585-10795A=	NP_003025.1:n.585-10795A=
XR_931322.1:n.1041+36173A=
NM_001304450.2:c.156-10795A=	NP_001291379.1:n.156-10795A=
NM_003034.4:c.585-10795A= MANE Select	NP_003025.1:n.585-10795A=