Canonical Allele Identifier: CA408701389

Gene: GSS

Linked Data

• MyVariant Identifiers: chr20:g.33519927C>A (hg19) ; chr20:g.34932124C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34932124C>A , CM000682.2:g.34932124C>A	GRCh38
NC_000020.10:g.33519927C>A , CM000682.1:g.33519927C>A	GRCh37
NC_000020.9:g.32983588C>A	NCBI36
NG_008848.1:g.28675G>T
NG_008848.2:g.28904G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000642493.1:c.*484G>T	ENSP00000493524.1:n.*484G>T
ENST00000642498.1:c.844G>T	ENSP00000493631.1:p.Ala282Ser
ENST00000642538.1:c.*188G>T	ENSP00000493927.1:n.*188G>T
ENST00000643188.1:c.844G>T	ENSP00000493903.1:p.Ala282Ser
ENST00000643443.1:c.*551G>T	ENSP00000495572.1:n.*551G>T
ENST00000643502.1:c.501G>T
ENST00000643908.1:n.1062G>T
ENST00000644538.1:n.1121G>T
ENST00000644793.1:c.844G>T	ENSP00000495750.1:p.Ala282Ser
ENST00000645328.1:c.222G>T
ENST00000645408.1:c.377G>T
ENST00000645723.1:n.2083G>T
ENST00000646405.1:c.*262G>T	ENSP00000493744.1:n.*262G>T
ENST00000646497.1:n.789G>T
ENST00000646512.1:n.990G>T
ENST00000646735.1:c.511G>T	ENSP00000493763.1:p.Ala171Ser
ENST00000651619.1:c.844G>T MANE Select	ENSP00000498303.1:p.Ala282Ser
ENST00000216951.6:c.844G>T	ENSP00000216951.2:p.Ala282Ser
ENST00000451957.2:c.511G>T	ENSP00000407517.2:p.Ala171Ser
NM_000178.2:c.844G>T	NP_000169.1:p.Ala282Ser
XM_005260406.3:c.844G>T	XP_005260463.1:p.Ala282Ser
XM_011528796.1:c.844G>T	XP_011527098.1:p.Ala282Ser
NM_000178.4:c.844G>T MANE Select	NP_000169.1:p.Ala282Ser
NM_001322494.1:c.844G>T	NP_001309423.1:p.Ala282Ser
NM_001322495.1:c.844G>T	NP_001309424.1:p.Ala282Ser