Canonical Allele Identifier: CA2361423036

Gene: GSS

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34932046G= , CM000682.2:g.34932046G=	GRCh38
NC_000020.10:g.33519849G= , CM000682.1:g.33519849G=	GRCh37
NC_000020.9:g.32983510G=	NCBI36
NG_008848.1:g.28753C=
NG_008848.2:g.28982C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642493.1:c.*562C=	ENSP00000493524.1:n.*562C=
ENST00000642498.1:c.922C=	ENSP00000493631.1:p.Gln308=
ENST00000642538.1:c.*266C=	ENSP00000493927.1:n.*266C=
ENST00000643188.1:c.922C=	ENSP00000493903.1:p.Gln308=
ENST00000643443.1:c.*629C=	ENSP00000495572.1:n.*629C=
ENST00000643502.1:c.579C=
ENST00000643908.1:n.1140C=
ENST00000644538.1:n.1199C=
ENST00000644793.1:c.922C=	ENSP00000495750.1:p.Gln308=
ENST00000645328.1:c.300C=
ENST00000645408.1:c.455C=
ENST00000645723.1:n.2161C=
ENST00000646405.1:c.*340C=	ENSP00000493744.1:n.*340C=
ENST00000646497.1:n.867C=
ENST00000646512.1:n.1068C=
ENST00000646735.1:c.589C=	ENSP00000493763.1:p.Gln197=
ENST00000651619.1:c.922C= MANE Select	ENSP00000498303.1:p.Gln308=
ENST00000216951.6:c.922C=	ENSP00000216951.2:p.Gln308=
ENST00000451957.2:c.589C=	ENSP00000407517.2:p.Gln197=
NM_000178.2:c.922C=	NP_000169.1:p.Gln308=
XM_005260406.3:c.922C=	XP_005260463.1:p.Gln308=
XM_011528796.1:c.922C=	XP_011527098.1:p.Gln308=
NM_000178.4:c.922C= MANE Select	NP_000169.1:p.Gln308=
NM_001322494.1:c.922C=	NP_001309423.1:p.Gln308=
NM_001322495.1:c.922C=	NP_001309424.1:p.Gln308=