Canonical Allele Identifier: CA408701027

Gene: GSS

Linked Data

• MyVariant Identifiers: chr20:g.33519753A>T (hg19) ; chr20:g.34931950A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34931950A>T , CM000682.2:g.34931950A>T	GRCh38
NC_000020.10:g.33519753A>T , CM000682.1:g.33519753A>T	GRCh37
NC_000020.9:g.32983414A>T	NCBI36
NG_008848.1:g.28849T>A
NG_008848.2:g.29078T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642498.1:c.1018T>A	ENSP00000493631.1:p.Ser340Thr
ENST00000642538.1:c.*362T>A	ENSP00000493927.1:n.*362T>A
ENST00000643188.1:c.1018T>A	ENSP00000493903.1:p.Ser340Thr
ENST00000643443.1:c.*725T>A	ENSP00000495572.1:n.*725T>A
ENST00000643502.1:c.675T>A
ENST00000643908.1:n.1236T>A
ENST00000644538.1:n.1295T>A
ENST00000644793.1:c.1018T>A	ENSP00000495750.1:p.Ser340Thr
ENST00000645328.1:c.396T>A
ENST00000645408.1:c.551T>A
ENST00000645723.1:n.2257T>A
ENST00000646405.1:c.*436T>A	ENSP00000493744.1:n.*436T>A
ENST00000646512.1:n.1164T>A
ENST00000646735.1:c.685T>A	ENSP00000493763.1:p.Ser229Thr
ENST00000651619.1:c.1018T>A MANE Select	ENSP00000498303.1:p.Ser340Thr
ENST00000216951.6:c.1018T>A	ENSP00000216951.2:p.Ser340Thr
ENST00000451957.2:c.685T>A	ENSP00000407517.2:p.Ser229Thr
NM_000178.2:c.1018T>A	NP_000169.1:p.Ser340Thr
XM_005260406.3:c.1018T>A	XP_005260463.1:p.Ser340Thr
XM_011528796.1:c.1018T>A	XP_011527098.1:p.Ser340Thr
NM_000178.4:c.1018T>A MANE Select	NP_000169.1:p.Ser340Thr
NM_001322494.1:c.1018T>A	NP_001309423.1:p.Ser340Thr
NM_001322495.1:c.1018T>A	NP_001309424.1:p.Ser340Thr