Canonical Allele Identifier: CA2361424437

Gene: GSS

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34935619A= , CM000682.2:g.34935619A=	GRCh38
NC_000020.10:g.33523422A= , CM000682.1:g.33523422A=	GRCh37
NC_000020.9:g.32987083A=	NCBI36
NG_008848.1:g.25180T=
NG_008848.2:g.25409T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000642493.1:c.*474+1144T=	ENSP00000493524.1:n.*474+1144T=
ENST00000642498.1:c.791T=	ENSP00000493631.1:p.Val264=
ENST00000642538.1:c.*135T=	ENSP00000493927.1:n.*135T=
ENST00000643188.1:c.791T=	ENSP00000493903.1:p.Val264=
ENST00000643443.1:c.*498T=	ENSP00000495572.1:n.*498T=
ENST00000643502.1:c.448T=
ENST00000643908.1:n.1052+1324T=
ENST00000644538.1:n.1068T=
ENST00000644793.1:c.791T=	ENSP00000495750.1:p.Val264=
ENST00000645328.1:c.169T=
ENST00000645408.1:c.367+1144T=
ENST00000645723.1:n.2030T=
ENST00000646405.1:c.*252+1144T=	ENSP00000493744.1:n.*252+1144T=
ENST00000646497.1:n.736T=
ENST00000646502.1:n.1273T=
ENST00000646512.1:n.980+1144T=
ENST00000646735.1:c.458T=	ENSP00000493763.1:p.Val153=
ENST00000646766.1:c.*421T=	ENSP00000494333.1:n.*421T=
ENST00000651619.1:c.791T= MANE Select	ENSP00000498303.1:p.Val264=
ENST00000216951.6:c.791T=	ENSP00000216951.2:p.Val264=
ENST00000451957.2:c.458T=	ENSP00000407517.2:p.Val153=
NM_000178.2:c.791T=	NP_000169.1:p.Val264=
XM_005260406.3:c.791T=	XP_005260463.1:p.Val264=
XM_011528796.1:c.791T=	XP_011527098.1:p.Val264=
NM_000178.4:c.791T= MANE Select	NP_000169.1:p.Val264=
NM_001322494.1:c.791T=	NP_001309423.1:p.Val264=
NM_001322495.1:c.791T=	NP_001309424.1:p.Val264=