Canonical Allele Identifier: CA2361423028
Gene: GSS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.34932025C= , CM000682.2:g.34932025C= GRCh38
NC_000020.10:g.33519828C= , CM000682.1:g.33519828C= GRCh37
NC_000020.9:g.32983489C= NCBI36
NG_008848.1:g.28774G=
NG_008848.2:g.29003G=

Transcript Alleles

HGVS Amino-acid change
ENST00000642498.1:c.943G= ENSP00000493631.1:p.Gly315=
ENST00000642538.1:c.*287G= ENSP00000493927.1:n.*287G=
ENST00000643188.1:c.943G= ENSP00000493903.1:p.Gly315=
ENST00000643443.1:c.*650G= ENSP00000495572.1:n.*650G=
ENST00000643502.1:c.600G=
ENST00000643908.1:n.1161G=
ENST00000644538.1:n.1220G=
ENST00000644793.1:c.943G= ENSP00000495750.1:p.Gly315=
ENST00000645328.1:c.321G=
ENST00000645408.1:c.476G=
ENST00000645723.1:n.2182G=
ENST00000646405.1:c.*361G= ENSP00000493744.1:n.*361G=
ENST00000646497.1:n.888G=
ENST00000646512.1:n.1089G=
ENST00000646735.1:c.610G= ENSP00000493763.1:p.Gly204=
ENST00000651619.1:c.943G= MANE Select ENSP00000498303.1:p.Gly315=
ENST00000216951.6:c.943G= ENSP00000216951.2:p.Gly315=
ENST00000451957.2:c.610G= ENSP00000407517.2:p.Gly204=
NM_000178.2:c.943G= NP_000169.1:p.Gly315=
XM_005260406.3:c.943G= XP_005260463.1:p.Gly315=
XM_011528796.1:c.943G= XP_011527098.1:p.Gly315=
NM_000178.4:c.943G= MANE Select NP_000169.1:p.Gly315=
NM_001322494.1:c.943G= NP_001309423.1:p.Gly315=
NM_001322495.1:c.943G= NP_001309424.1:p.Gly315=