Canonical Allele Identifier: CA1669582433

Gene: STX11

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.144186661T= , CM000668.2:g.144186661T=	GRCh38
NC_000006.11:g.144507798T= , CM000668.1:g.144507798T=	GRCh37
NC_000006.10:g.144549491T=	NCBI36
NG_007613.1:g.41145T= , LRG_113:g.41145T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698355.1:c.34T=	ENSP00000513678.1:p.Ser12=
ENST00000698356.1:c.34T=	ENSP00000513679.1:p.Ser12=
ENST00000698357.1:c.34T=	ENSP00000513680.1:p.Ser12=
ENST00000367568.5:c.34T= MANE Select	ENSP00000356540.4:p.Ser12=
ENST00000367568.4:c.34T=	ENSP00000356540.4:p.Ser12=
NM_003764.3:c.34T= , LRG_113t1:c.34T=	NP_003755.2:p.Ser12=
XM_011536213.1:c.112T=	XP_011534515.1:p.Ser38=
XM_011536214.1:c.34T=	XP_011534516.1:p.Ser12=
XM_011536215.1:c.34T=	XP_011534517.1:p.Ser12=
XM_011536216.1:c.34T=	XP_011534518.1:p.Ser12=
XM_011536217.1:c.34T=	XP_011534519.1:p.Ser12=
XM_011536218.1:c.34T=	XP_011534520.1:p.Ser12=
XM_011536213.2:c.112T=	XP_011534515.1:p.Ser38=
XM_011536214.2:c.34T=	XP_011534516.1:p.Ser12=
XM_011536217.2:c.34T=	XP_011534519.1:p.Ser12=
XM_011536218.2:c.34T=	XP_011534520.1:p.Ser12=
XM_017011400.1:c.34T=	XP_016866889.1:p.Ser12=
NM_003764.4:c.34T= MANE Select	NP_003755.2:p.Ser12=