Canonical Allele Identifier: CA2361423076

Gene: GSS

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34932185C= , CM000682.2:g.34932185C=	GRCh38
NC_000020.10:g.33519988C= , CM000682.1:g.33519988C=	GRCh37
NC_000020.9:g.32983649C=	NCBI36
NG_008848.1:g.28614G=
NG_008848.2:g.28843G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642493.1:c.*475-52G=	ENSP00000493524.1:n.*475-52G=
ENST00000642498.1:c.835-52G=	ENSP00000493631.1:n.835-52G=
ENST00000642538.1:c.*179-52G=	ENSP00000493927.1:n.*179-52G=
ENST00000643188.1:c.835-52G=	ENSP00000493903.1:n.835-52G=
ENST00000643443.1:c.*542-52G=	ENSP00000495572.1:n.*542-52G=
ENST00000643502.1:c.492-52G=
ENST00000643908.1:n.1053-52G=
ENST00000644538.1:n.1112-52G=
ENST00000644793.1:c.835-52G=	ENSP00000495750.1:n.835-52G=
ENST00000645328.1:c.213-52G=
ENST00000645408.1:c.368-52G=
ENST00000645723.1:n.2074-52G=
ENST00000646405.1:c.*253-52G=	ENSP00000493744.1:n.*253-52G=
ENST00000646497.1:n.780-52G=
ENST00000646512.1:n.981-52G=
ENST00000646735.1:c.502-52G=	ENSP00000493763.1:n.502-52G=
ENST00000651619.1:c.835-52G= MANE Select	ENSP00000498303.1:n.835-52G=
ENST00000216951.6:c.835-52G=	ENSP00000216951.2:n.835-52G=
ENST00000451957.2:c.502-52G=	ENSP00000407517.2:n.502-52G=
NM_000178.2:c.835-52G=	NP_000169.1:n.835-52G=
XM_005260406.3:c.835-52G=	XP_005260463.1:n.835-52G=
XM_011528796.1:c.835-52G=	XP_011527098.1:n.835-52G=
NM_000178.4:c.835-52G= MANE Select	NP_000169.1:n.835-52G=
NM_001322494.1:c.835-52G=	NP_001309423.1:n.835-52G=
NM_001322495.1:c.835-52G=	NP_001309424.1:n.835-52G=