Canonical Allele Identifier: CA686456532

Gene: ST8SIA1

Linked Data

• dbSNP Id: rs1173415983
• gnomAD v3: 12-22212936-A-G
• gnomAD v4: 12-22212936-A-G
• MyVariant Identifiers: chr12:g.22365870A>G (hg19) ; chr12:g.22212936A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.22212936A>G , CM000674.2:g.22212936A>G	GRCh38
NC_000012.11:g.22365870A>G , CM000674.1:g.22365870A>G	GRCh37
NC_000012.10:g.22257137A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000396037.9:c.585-10898T>C MANE Select	ENSP00000379353.3:n.585-10898T>C
ENST00000261197.7:c.*67-10898T>C	ENSP00000261197.3:n.*67-10898T>C
ENST00000396037.8:c.585-10898T>C	ENSP00000379353.3:n.585-10898T>C
ENST00000508924.2:n.188-10898T>C
ENST00000540824.5:c.438-10898T>C	ENSP00000441707.1:n.438-10898T>C
ENST00000544732.5:n.151+36070T>C
ENST00000545494.5:n.306-10898T>C
ENST00000545524.5:n.249+36070T>C
NM_001304450.1:c.156-10898T>C	NP_001291379.1:n.156-10898T>C
NM_003034.3:c.585-10898T>C	NP_003025.1:n.585-10898T>C
XR_931322.1:n.1041+36070T>C
NM_001304450.2:c.156-10898T>C	NP_001291379.1:n.156-10898T>C
NM_003034.4:c.585-10898T>C MANE Select	NP_003025.1:n.585-10898T>C