Canonical Allele Identifier: CA408702433

Gene: GSS

Linked Data

• MyVariant Identifiers: chr20:g.33523442A>C (hg19) ; chr20:g.34935639A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34935639A>C , CM000682.2:g.34935639A>C	GRCh38
NC_000020.10:g.33523442A>C , CM000682.1:g.33523442A>C	GRCh37
NC_000020.9:g.32987103A>C	NCBI36
NG_008848.1:g.25160T>G
NG_008848.2:g.25389T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642493.1:c.*474+1124T>G	ENSP00000493524.1:n.*474+1124T>G
ENST00000642498.1:c.771T>G	ENSP00000493631.1:p.Asp257Glu
ENST00000642538.1:c.*115T>G	ENSP00000493927.1:n.*115T>G
ENST00000643188.1:c.771T>G	ENSP00000493903.1:p.Asp257Glu
ENST00000643443.1:c.*478T>G	ENSP00000495572.1:n.*478T>G
ENST00000643502.1:c.428T>G
ENST00000643908.1:n.1052+1304T>G
ENST00000644538.1:n.1048T>G
ENST00000644793.1:c.771T>G	ENSP00000495750.1:p.Asp257Glu
ENST00000645328.1:c.149T>G
ENST00000645408.1:c.367+1124T>G
ENST00000645723.1:n.2010T>G
ENST00000646405.1:c.*252+1124T>G	ENSP00000493744.1:n.*252+1124T>G
ENST00000646497.1:n.716T>G
ENST00000646502.1:n.1253T>G
ENST00000646512.1:n.980+1124T>G
ENST00000646735.1:c.438T>G	ENSP00000493763.1:p.Asp146Glu
ENST00000646766.1:c.*401T>G	ENSP00000494333.1:n.*401T>G
ENST00000651619.1:c.771T>G MANE Select	ENSP00000498303.1:p.Asp257Glu
ENST00000216951.6:c.771T>G	ENSP00000216951.2:p.Asp257Glu
ENST00000451957.2:c.438T>G	ENSP00000407517.2:p.Asp146Glu
NM_000178.2:c.771T>G	NP_000169.1:p.Asp257Glu
XM_005260406.3:c.771T>G	XP_005260463.1:p.Asp257Glu
XM_011528796.1:c.771T>G	XP_011527098.1:p.Asp257Glu
NM_000178.4:c.771T>G MANE Select	NP_000169.1:p.Asp257Glu
NM_001322494.1:c.771T>G	NP_001309423.1:p.Asp257Glu
NM_001322495.1:c.771T>G	NP_001309424.1:p.Asp257Glu