Canonical Allele Identifier: CA2361424441

Gene: GSS

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34935625G= , CM000682.2:g.34935625G=	GRCh38
NC_000020.10:g.33523428G= , CM000682.1:g.33523428G=	GRCh37
NC_000020.9:g.32987089G=	NCBI36
NG_008848.1:g.25174C=
NG_008848.2:g.25403C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642493.1:c.*474+1138C=	ENSP00000493524.1:n.*474+1138C=
ENST00000642498.1:c.785C=	ENSP00000493631.1:p.Ala262=
ENST00000642538.1:c.*129C=	ENSP00000493927.1:n.*129C=
ENST00000643188.1:c.785C=	ENSP00000493903.1:p.Ala262=
ENST00000643443.1:c.*492C=	ENSP00000495572.1:n.*492C=
ENST00000643502.1:c.442C=
ENST00000643908.1:n.1052+1318C=
ENST00000644538.1:n.1062C=
ENST00000644793.1:c.785C=	ENSP00000495750.1:p.Ala262=
ENST00000645328.1:c.163C=
ENST00000645408.1:c.367+1138C=
ENST00000645723.1:n.2024C=
ENST00000646405.1:c.*252+1138C=	ENSP00000493744.1:n.*252+1138C=
ENST00000646497.1:n.730C=
ENST00000646502.1:n.1267C=
ENST00000646512.1:n.980+1138C=
ENST00000646735.1:c.452C=	ENSP00000493763.1:p.Ala151=
ENST00000646766.1:c.*415C=	ENSP00000494333.1:n.*415C=
ENST00000651619.1:c.785C= MANE Select	ENSP00000498303.1:p.Ala262=
ENST00000216951.6:c.785C=	ENSP00000216951.2:p.Ala262=
ENST00000451957.2:c.452C=	ENSP00000407517.2:p.Ala151=
NM_000178.2:c.785C=	NP_000169.1:p.Ala262=
XM_005260406.3:c.785C=	XP_005260463.1:p.Ala262=
XM_011528796.1:c.785C=	XP_011527098.1:p.Ala262=
NM_000178.4:c.785C= MANE Select	NP_000169.1:p.Ala262=
NM_001322494.1:c.785C=	NP_001309423.1:p.Ala262=
NM_001322495.1:c.785C=	NP_001309424.1:p.Ala262=