Canonical Allele Identifier: CA2361423017

Gene: GSS

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34931995G= , CM000682.2:g.34931995G=	GRCh38
NC_000020.10:g.33519798G= , CM000682.1:g.33519798G=	GRCh37
NC_000020.9:g.32983459G=	NCBI36
NG_008848.1:g.28804C=
NG_008848.2:g.29033C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642498.1:c.973C=	ENSP00000493631.1:p.Pro325=
ENST00000642538.1:c.*317C=	ENSP00000493927.1:n.*317C=
ENST00000643188.1:c.973C=	ENSP00000493903.1:p.Pro325=
ENST00000643443.1:c.*680C=	ENSP00000495572.1:n.*680C=
ENST00000643502.1:c.630C=
ENST00000643908.1:n.1191C=
ENST00000644538.1:n.1250C=
ENST00000644793.1:c.973C=	ENSP00000495750.1:p.Pro325=
ENST00000645328.1:c.351C=
ENST00000645408.1:c.506C=
ENST00000645723.1:n.2212C=
ENST00000646405.1:c.*391C=	ENSP00000493744.1:n.*391C=
ENST00000646512.1:n.1119C=
ENST00000646735.1:c.640C=	ENSP00000493763.1:p.Pro214=
ENST00000651619.1:c.973C= MANE Select	ENSP00000498303.1:p.Pro325=
ENST00000216951.6:c.973C=	ENSP00000216951.2:p.Pro325=
ENST00000451957.2:c.640C=	ENSP00000407517.2:p.Pro214=
NM_000178.2:c.973C=	NP_000169.1:p.Pro325=
XM_005260406.3:c.973C=	XP_005260463.1:p.Pro325=
XM_011528796.1:c.973C=	XP_011527098.1:p.Pro325=
NM_000178.4:c.973C= MANE Select	NP_000169.1:p.Pro325=
NM_001322494.1:c.973C=	NP_001309423.1:p.Pro325=
NM_001322495.1:c.973C=	NP_001309424.1:p.Pro325=