Canonical Allele Identifier: CA1933343508
Gene: STN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103900039T= , CM000672.2:g.103900039T= GRCh38
NC_000010.10:g.105659797T= , CM000672.1:g.105659797T= GRCh37
NC_000010.9:g.105649787T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369764.2:c.457+23A= ENSP00000358779.1:n.457+23A=
ENST00000466828.6:c.457+23A= ENSP00000513624.1:n.457+23A=
ENST00000698241.1:c.457+23A= ENSP00000513621.1:n.457+23A=
ENST00000698242.1:c.457+23A= ENSP00000513622.1:n.457+23A=
ENST00000698243.1:c.457+23A= ENSP00000513623.1:n.457+23A=
ENST00000698245.1:c.457+23A= ENSP00000513626.1:n.457+23A=
ENST00000698246.1:c.457+23A= ENSP00000513627.1:n.457+23A=
ENST00000698297.1:c.457+23A= ENSP00000513657.1:n.457+23A=
ENST00000698298.1:c.457+23A= ENSP00000513658.1:n.457+23A=
ENST00000698299.1:c.457+23A= ENSP00000513659.1:n.457+23A=
ENST00000698300.1:c.457+23A= ENSP00000513660.1:n.457+23A=
ENST00000698301.1:c.-42+23A= ENSP00000513661.1:n.-42+23A=
ENST00000698302.1:c.*294+23A= ENSP00000513662.1:n.*294+23A=
ENST00000698303.1:c.361+23A= ENSP00000513663.1:n.361+23A=
ENST00000698304.1:c.457+23A= ENSP00000513664.1:n.457+23A=
ENST00000698305.1:c.457+23A= ENSP00000513665.1:n.457+23A=
ENST00000698328.1:c.457+23A= ENSP00000513669.1:n.457+23A=
ENST00000224950.8:c.457+23A= MANE Select ENSP00000224950.3:n.457+23A=
ENST00000224950.7:c.457+23A= ENSP00000224950.3:n.457+23A=
ENST00000369764.1:c.457+23A= ENSP00000358779.1:n.457+23A=
ENST00000466828.5:n.550+23A=
ENST00000472951.1:n.115A=
NM_024928.4:c.457+23A= NP_079204.2:n.457+23A=
XM_006717976.2:c.457+23A= XP_006718039.1:n.457+23A=
XM_011540184.1:c.457+23A= XP_011538486.1:n.457+23A=
NM_024928.5:c.457+23A= MANE Select NP_079204.2:n.457+23A=