Canonical Allele Identifier: CA2361423038

Gene: GSS

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34932052T= , CM000682.2:g.34932052T=	GRCh38
NC_000020.10:g.33519855T= , CM000682.1:g.33519855T=	GRCh37
NC_000020.9:g.32983516T=	NCBI36
NG_008848.1:g.28747A=
NG_008848.2:g.28976A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642493.1:c.*556A=	ENSP00000493524.1:n.*556A=
ENST00000642498.1:c.916A=	ENSP00000493631.1:p.Lys306=
ENST00000642538.1:c.*260A=	ENSP00000493927.1:n.*260A=
ENST00000643188.1:c.916A=	ENSP00000493903.1:p.Lys306=
ENST00000643443.1:c.*623A=	ENSP00000495572.1:n.*623A=
ENST00000643502.1:c.573A=
ENST00000643908.1:n.1134A=
ENST00000644538.1:n.1193A=
ENST00000644793.1:c.916A=	ENSP00000495750.1:p.Lys306=
ENST00000645328.1:c.294A=
ENST00000645408.1:c.449A=
ENST00000645723.1:n.2155A=
ENST00000646405.1:c.*334A=	ENSP00000493744.1:n.*334A=
ENST00000646497.1:n.861A=
ENST00000646512.1:n.1062A=
ENST00000646735.1:c.583A=	ENSP00000493763.1:p.Lys195=
ENST00000651619.1:c.916A= MANE Select	ENSP00000498303.1:p.Lys306=
ENST00000216951.6:c.916A=	ENSP00000216951.2:p.Lys306=
ENST00000451957.2:c.583A=	ENSP00000407517.2:p.Lys195=
NM_000178.2:c.916A=	NP_000169.1:p.Lys306=
XM_005260406.3:c.916A=	XP_005260463.1:p.Lys306=
XM_011528796.1:c.916A=	XP_011527098.1:p.Lys306=
NM_000178.4:c.916A= MANE Select	NP_000169.1:p.Lys306=
NM_001322494.1:c.916A=	NP_001309423.1:p.Lys306=
NM_001322495.1:c.916A=	NP_001309424.1:p.Lys306=