Canonical Allele Identifier: CA1933331519

Gene: STN1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.103887337G= , CM000672.2:g.103887337G=	GRCh38
NC_000010.10:g.105647095G= , CM000672.1:g.105647095G=	GRCh37
NC_000010.9:g.105637085G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_024928.5:c.949+1735C= MANE Select	NP_079204.2:n.949+1735C=
ENST00000224950.8:c.949+1735C= MANE Select	ENSP00000224950.3:n.949+1735C=
NM_024928.4:c.949+1735C=	NP_079204.2:n.949+1735C=
ENST00000224950.7:c.949+1735C=	ENSP00000224950.3:n.949+1735C=
ENST00000369764.1:c.949+1735C=	ENSP00000358779.1:n.949+1735C=
ENST00000369764.2:c.949+1735C=	ENSP00000358779.1:n.949+1735C=
ENST00000466828.5:n.1127+1735C=
ENST00000466828.6:c.*398+1735C=	ENSP00000513624.1:n.*398+1735C=
ENST00000472951.1:n.686+1735C=
ENST00000698241.1:c.949+1735C=	ENSP00000513621.1:n.949+1735C=
ENST00000698242.1:c.949+1735C=	ENSP00000513622.1:n.949+1735C=
ENST00000698243.1:c.949+1735C=	ENSP00000513623.1:n.949+1735C=
ENST00000698244.1:n.324+1735C=
ENST00000698245.1:c.*288C=	ENSP00000513626.1:n.*288C=
ENST00000698246.1:c.*288C=	ENSP00000513627.1:n.*288C=
ENST00000698297.1:c.949+1735C=	ENSP00000513657.1:n.949+1735C=
ENST00000698298.1:c.949+1735C=	ENSP00000513658.1:n.949+1735C=
ENST00000698299.1:c.949+1735C=	ENSP00000513659.1:n.949+1735C=
ENST00000698300.1:c.949+1735C=	ENSP00000513660.1:n.949+1735C=
ENST00000698301.1:c.451+1735C=	ENSP00000513661.1:n.451+1735C=
ENST00000698302.1:c.*786+1735C=	ENSP00000513662.1:n.*786+1735C=
ENST00000698303.1:c.853+1735C=	ENSP00000513663.1:n.853+1735C=
ENST00000698304.1:c.949+1735C=	ENSP00000513664.1:n.949+1735C=
ENST00000698305.1:c.949+1735C=	ENSP00000513665.1:n.949+1735C=
ENST00000698328.1:c.*1613C=	ENSP00000513669.1:n.*1613C=
XM_006717976.2:c.949+1735C=	XP_006718039.1:n.949+1735C=
XM_011540184.1:c.*288C=	XP_011538486.1:n.*288C=