Canonical Allele Identifier: CA408701278

Gene: GSS

Linked Data

• MyVariant Identifiers: chr20:g.33519875G>C (hg19) ; chr20:g.34932072G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34932072G>C , CM000682.2:g.34932072G>C	GRCh38
NC_000020.10:g.33519875G>C , CM000682.1:g.33519875G>C	GRCh37
NC_000020.9:g.32983536G>C	NCBI36
NG_008848.1:g.28727C>G
NG_008848.2:g.28956C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642493.1:c.*536C>G	ENSP00000493524.1:n.*536C>G
ENST00000642498.1:c.896C>G	ENSP00000493631.1:p.Thr299Ser
ENST00000642538.1:c.*240C>G	ENSP00000493927.1:n.*240C>G
ENST00000643188.1:c.896C>G	ENSP00000493903.1:p.Thr299Ser
ENST00000643443.1:c.*603C>G	ENSP00000495572.1:n.*603C>G
ENST00000643502.1:c.553C>G
ENST00000643908.1:n.1114C>G
ENST00000644538.1:n.1173C>G
ENST00000644793.1:c.896C>G	ENSP00000495750.1:p.Thr299Ser
ENST00000645328.1:c.274C>G
ENST00000645408.1:c.429C>G
ENST00000645723.1:n.2135C>G
ENST00000646405.1:c.*314C>G	ENSP00000493744.1:n.*314C>G
ENST00000646497.1:n.841C>G
ENST00000646512.1:n.1042C>G
ENST00000646735.1:c.563C>G	ENSP00000493763.1:p.Thr188Ser
ENST00000651619.1:c.896C>G MANE Select	ENSP00000498303.1:p.Thr299Ser
ENST00000216951.6:c.896C>G	ENSP00000216951.2:p.Thr299Ser
ENST00000451957.2:c.563C>G	ENSP00000407517.2:p.Thr188Ser
NM_000178.2:c.896C>G	NP_000169.1:p.Thr299Ser
XM_005260406.3:c.896C>G	XP_005260463.1:p.Thr299Ser
XM_011528796.1:c.896C>G	XP_011527098.1:p.Thr299Ser
NM_000178.4:c.896C>G MANE Select	NP_000169.1:p.Thr299Ser
NM_001322494.1:c.896C>G	NP_001309423.1:p.Thr299Ser
NM_001322495.1:c.896C>G	NP_001309424.1:p.Thr299Ser