Canonical Allele Identifier: CA16400347

Gene: STN1

Linked Data

• dbSNP Id: rs4387287
• gnomAD v2: 10-105677897-A-C
• gnomAD v3: 10-103918139-A-C
• gnomAD v4: 10-103918139-A-C
• MyVariant Identifiers: chr10:g.105677897A>C (hg19) ; chr10:g.103918139A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.103918139A>C , CM000672.2:g.103918139A>C	GRCh38
NC_000010.10:g.105677897A>C , CM000672.1:g.105677897A>C	GRCh37
NC_000010.9:g.105667887A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369764.2:c.-545T>G	ENSP00000358779.1:n.-545T>G
ENST00000466828.6:c.-102T>G	ENSP00000513624.1:n.-102T>G
ENST00000698241.1:c.-63+125T>G	ENSP00000513621.1:n.-63+125T>G
ENST00000698242.1:c.-102T>G	ENSP00000513622.1:n.-102T>G
ENST00000698243.1:c.-63+125T>G	ENSP00000513623.1:n.-63+125T>G
ENST00000698245.1:c.-63+125T>G	ENSP00000513626.1:n.-63+125T>G
ENST00000698246.1:c.-102T>G	ENSP00000513627.1:n.-102T>G
ENST00000698297.1:c.-63+4T>G	ENSP00000513657.1:n.-63+4T>G
ENST00000698298.1:c.-102T>G	ENSP00000513658.1:n.-102T>G
ENST00000698299.1:c.-545T>G	ENSP00000513659.1:n.-545T>G
ENST00000698300.1:c.-102T>G	ENSP00000513660.1:n.-102T>G
ENST00000698305.1:c.-102T>G	ENSP00000513665.1:n.-102T>G
ENST00000698328.1:c.-102T>G	ENSP00000513669.1:n.-102T>G
ENST00000224950.8:c.-102T>G MANE Select	ENSP00000224950.3:n.-102T>G
ENST00000224950.7:c.-102T>G	ENSP00000224950.3:n.-102T>G
NM_024928.4:c.-102T>G	NP_079204.2:n.-102T>G
XM_006717976.2:c.-102T>G	XP_006718039.1:n.-102T>G
XM_011540184.1:c.-102T>G	XP_011538486.1:n.-102T>G
NM_024928.5:c.-102T>G MANE Select	NP_079204.2:n.-102T>G