Canonical Allele Identifier: CA408701361

Gene: GSS

Linked Data

• MyVariant Identifiers: chr20:g.33519911T>C (hg19) ; chr20:g.34932108T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34932108T>C , CM000682.2:g.34932108T>C	GRCh38
NC_000020.10:g.33519911T>C , CM000682.1:g.33519911T>C	GRCh37
NC_000020.9:g.32983572T>C	NCBI36
NG_008848.1:g.28691A>G
NG_008848.2:g.28920A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642493.1:c.*500A>G	ENSP00000493524.1:n.*500A>G
ENST00000642498.1:c.860A>G	ENSP00000493631.1:p.Glu287Gly
ENST00000642538.1:c.*204A>G	ENSP00000493927.1:n.*204A>G
ENST00000643188.1:c.860A>G	ENSP00000493903.1:p.Glu287Gly
ENST00000643443.1:c.*567A>G	ENSP00000495572.1:n.*567A>G
ENST00000643502.1:c.517A>G
ENST00000643908.1:n.1078A>G
ENST00000644538.1:n.1137A>G
ENST00000644793.1:c.860A>G	ENSP00000495750.1:p.Glu287Gly
ENST00000645328.1:c.238A>G
ENST00000645408.1:c.393A>G
ENST00000645723.1:n.2099A>G
ENST00000646405.1:c.*278A>G	ENSP00000493744.1:n.*278A>G
ENST00000646497.1:n.805A>G
ENST00000646512.1:n.1006A>G
ENST00000646735.1:c.527A>G	ENSP00000493763.1:p.Glu176Gly
ENST00000651619.1:c.860A>G MANE Select	ENSP00000498303.1:p.Glu287Gly
ENST00000216951.6:c.860A>G	ENSP00000216951.2:p.Glu287Gly
ENST00000451957.2:c.527A>G	ENSP00000407517.2:p.Glu176Gly
NM_000178.2:c.860A>G	NP_000169.1:p.Glu287Gly
XM_005260406.3:c.860A>G	XP_005260463.1:p.Glu287Gly
XM_011528796.1:c.860A>G	XP_011527098.1:p.Glu287Gly
NM_000178.4:c.860A>G MANE Select	NP_000169.1:p.Glu287Gly
NM_001322494.1:c.860A>G	NP_001309423.1:p.Glu287Gly
NM_001322495.1:c.860A>G	NP_001309424.1:p.Glu287Gly