Canonical Allele Identifier: CA2361424444

Gene: GSS

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34935636G= , CM000682.2:g.34935636G=	GRCh38
NC_000020.10:g.33523439G= , CM000682.1:g.33523439G=	GRCh37
NC_000020.9:g.32987100G=	NCBI36
NG_008848.1:g.25163C=
NG_008848.2:g.25392C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000642493.1:c.*474+1127C=	ENSP00000493524.1:n.*474+1127C=
ENST00000642498.1:c.774C=	ENSP00000493631.1:p.Gly258=
ENST00000642538.1:c.*118C=	ENSP00000493927.1:n.*118C=
ENST00000643188.1:c.774C=	ENSP00000493903.1:p.Gly258=
ENST00000643443.1:c.*481C=	ENSP00000495572.1:n.*481C=
ENST00000643502.1:c.431C=
ENST00000643908.1:n.1052+1307C=
ENST00000644538.1:n.1051C=
ENST00000644793.1:c.774C=	ENSP00000495750.1:p.Gly258=
ENST00000645328.1:c.152C=
ENST00000645408.1:c.367+1127C=
ENST00000645723.1:n.2013C=
ENST00000646405.1:c.*252+1127C=	ENSP00000493744.1:n.*252+1127C=
ENST00000646497.1:n.719C=
ENST00000646502.1:n.1256C=
ENST00000646512.1:n.980+1127C=
ENST00000646735.1:c.441C=	ENSP00000493763.1:p.Gly147=
ENST00000646766.1:c.*404C=	ENSP00000494333.1:n.*404C=
ENST00000651619.1:c.774C= MANE Select	ENSP00000498303.1:p.Gly258=
ENST00000216951.6:c.774C=	ENSP00000216951.2:p.Gly258=
ENST00000451957.2:c.441C=	ENSP00000407517.2:p.Gly147=
NM_000178.2:c.774C=	NP_000169.1:p.Gly258=
XM_005260406.3:c.774C=	XP_005260463.1:p.Gly258=
XM_011528796.1:c.774C=	XP_011527098.1:p.Gly258=
NM_000178.4:c.774C= MANE Select	NP_000169.1:p.Gly258=
NM_001322494.1:c.774C=	NP_001309423.1:p.Gly258=
NM_001322495.1:c.774C=	NP_001309424.1:p.Gly258=