Canonical Allele Identifier: CA2361423010

Gene: GSS

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34931978G= , CM000682.2:g.34931978G=	GRCh38
NC_000020.10:g.33519781G= , CM000682.1:g.33519781G=	GRCh37
NC_000020.9:g.32983442G=	NCBI36
NG_008848.1:g.28821C=
NG_008848.2:g.29050C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642498.1:c.990C=	ENSP00000493631.1:p.Arg330=
ENST00000642538.1:c.*334C=	ENSP00000493927.1:n.*334C=
ENST00000643188.1:c.990C=	ENSP00000493903.1:p.Arg330=
ENST00000643443.1:c.*697C=	ENSP00000495572.1:n.*697C=
ENST00000643502.1:c.647C=
ENST00000643908.1:n.1208C=
ENST00000644538.1:n.1267C=
ENST00000644793.1:c.990C=	ENSP00000495750.1:p.Arg330=
ENST00000645328.1:c.368C=
ENST00000645408.1:c.523C=
ENST00000645723.1:n.2229C=
ENST00000646405.1:c.*408C=	ENSP00000493744.1:n.*408C=
ENST00000646512.1:n.1136C=
ENST00000646735.1:c.657C=	ENSP00000493763.1:p.Arg219=
ENST00000651619.1:c.990C= MANE Select	ENSP00000498303.1:p.Arg330=
ENST00000216951.6:c.990C=	ENSP00000216951.2:p.Arg330=
ENST00000451957.2:c.657C=	ENSP00000407517.2:p.Arg219=
NM_000178.2:c.990C=	NP_000169.1:p.Arg330=
XM_005260406.3:c.990C=	XP_005260463.1:p.Arg330=
XM_011528796.1:c.990C=	XP_011527098.1:p.Arg330=
NM_000178.4:c.990C= MANE Select	NP_000169.1:p.Arg330=
NM_001322494.1:c.990C=	NP_001309423.1:p.Arg330=
NM_001322495.1:c.990C=	NP_001309424.1:p.Arg330=