Canonical Allele Identifier: CA408701171

Gene: GSS

Linked Data

• MyVariant Identifiers: chr20:g.33519825T>A (hg19) ; chr20:g.34932022T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34932022T>A , CM000682.2:g.34932022T>A	GRCh38
NC_000020.10:g.33519825T>A , CM000682.1:g.33519825T>A	GRCh37
NC_000020.9:g.32983486T>A	NCBI36
NG_008848.1:g.28777A>T
NG_008848.2:g.29006A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642498.1:c.946A>T	ENSP00000493631.1:p.Met316Leu
ENST00000642538.1:c.*290A>T	ENSP00000493927.1:n.*290A>T
ENST00000643188.1:c.946A>T	ENSP00000493903.1:p.Met316Leu
ENST00000643443.1:c.*653A>T	ENSP00000495572.1:n.*653A>T
ENST00000643502.1:c.603A>T
ENST00000643908.1:n.1164A>T
ENST00000644538.1:n.1223A>T
ENST00000644793.1:c.946A>T	ENSP00000495750.1:p.Met316Leu
ENST00000645328.1:c.324A>T
ENST00000645408.1:c.479A>T
ENST00000645723.1:n.2185A>T
ENST00000646405.1:c.*364A>T	ENSP00000493744.1:n.*364A>T
ENST00000646497.1:n.891A>T
ENST00000646512.1:n.1092A>T
ENST00000646735.1:c.613A>T	ENSP00000493763.1:p.Met205Leu
ENST00000651619.1:c.946A>T MANE Select	ENSP00000498303.1:p.Met316Leu
ENST00000216951.6:c.946A>T	ENSP00000216951.2:p.Met316Leu
ENST00000451957.2:c.613A>T	ENSP00000407517.2:p.Met205Leu
NM_000178.2:c.946A>T	NP_000169.1:p.Met316Leu
XM_005260406.3:c.946A>T	XP_005260463.1:p.Met316Leu
XM_011528796.1:c.946A>T	XP_011527098.1:p.Met316Leu
NM_000178.4:c.946A>T MANE Select	NP_000169.1:p.Met316Leu
NM_001322494.1:c.946A>T	NP_001309423.1:p.Met316Leu
NM_001322495.1:c.946A>T	NP_001309424.1:p.Met316Leu