Canonical Allele Identifier: CA408704187

Gene: GSS

Linked Data

• MyVariant Identifiers: chr20:g.33530300G>C (hg19) ; chr20:g.34942497G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34942497G>C , CM000682.2:g.34942497G>C	GRCh38
NC_000020.10:g.33530300G>C , CM000682.1:g.33530300G>C	GRCh37
NC_000020.9:g.32993961G>C	NCBI36
NG_008848.1:g.18302C>G
NG_008848.2:g.18531C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642493.1:c.*189C>G	ENSP00000493524.1:n.*189C>G
ENST00000642498.1:c.482C>G	ENSP00000493631.1:p.Ala161Gly
ENST00000642538.1:c.351+434C>G	ENSP00000493927.1:n.351+434C>G
ENST00000643188.1:c.482C>G	ENSP00000493903.1:p.Ala161Gly
ENST00000643443.1:c.*189C>G	ENSP00000495572.1:n.*189C>G
ENST00000643502.1:c.139C>G
ENST00000643908.1:n.845C>G
ENST00000644538.1:n.759C>G
ENST00000644793.1:c.482C>G	ENSP00000495750.1:p.Ala161Gly
ENST00000645408.1:c.82C>G
ENST00000645723.1:n.1721C>G
ENST00000646405.1:c.351+434C>G	ENSP00000493744.1:n.351+434C>G
ENST00000646497.1:n.429C>G
ENST00000646502.1:n.964C>G
ENST00000646512.1:n.695C>G
ENST00000646735.1:c.275+3456C>G	ENSP00000493763.1:n.275+3456C>G
ENST00000646766.1:c.*112C>G	ENSP00000494333.1:n.*112C>G
ENST00000651619.1:c.482C>G MANE Select	ENSP00000498303.1:p.Ala161Gly
ENST00000216951.6:c.482C>G	ENSP00000216951.2:p.Ala161Gly
ENST00000451957.2:c.275+3456C>G	ENSP00000407517.2:n.275+3456C>G
NM_000178.2:c.482C>G	NP_000169.1:p.Ala161Gly
XM_005260406.3:c.482C>G	XP_005260463.1:p.Ala161Gly
XM_011528796.1:c.482C>G	XP_011527098.1:p.Ala161Gly
NM_000178.4:c.482C>G MANE Select	NP_000169.1:p.Ala161Gly
NM_001322494.1:c.482C>G	NP_001309423.1:p.Ala161Gly
NM_001322495.1:c.482C>G	NP_001309424.1:p.Ala161Gly