Canonical Allele Identifier: CA408704216

Gene: GSS

Linked Data

• MyVariant Identifiers: chr20:g.33530307T>C (hg19) ; chr20:g.34942504T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34942504T>C , CM000682.2:g.34942504T>C	GRCh38
NC_000020.10:g.33530307T>C , CM000682.1:g.33530307T>C	GRCh37
NC_000020.9:g.32993968T>C	NCBI36
NG_008848.1:g.18295A>G
NG_008848.2:g.18524A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642493.1:c.*182A>G	ENSP00000493524.1:n.*182A>G
ENST00000642498.1:c.475A>G	ENSP00000493631.1:p.Thr159Ala
ENST00000642538.1:c.351+427A>G	ENSP00000493927.1:n.351+427A>G
ENST00000643188.1:c.475A>G	ENSP00000493903.1:p.Thr159Ala
ENST00000643443.1:c.*182A>G	ENSP00000495572.1:n.*182A>G
ENST00000643502.1:c.132A>G
ENST00000643908.1:n.838A>G
ENST00000644538.1:n.752A>G
ENST00000644793.1:c.475A>G	ENSP00000495750.1:p.Thr159Ala
ENST00000645408.1:c.75A>G
ENST00000645723.1:n.1714A>G
ENST00000646405.1:c.351+427A>G	ENSP00000493744.1:n.351+427A>G
ENST00000646497.1:n.422A>G
ENST00000646502.1:n.957A>G
ENST00000646512.1:n.688A>G
ENST00000646735.1:c.275+3449A>G	ENSP00000493763.1:n.275+3449A>G
ENST00000646766.1:c.*105A>G	ENSP00000494333.1:n.*105A>G
ENST00000651619.1:c.475A>G MANE Select	ENSP00000498303.1:p.Thr159Ala
ENST00000216951.6:c.475A>G	ENSP00000216951.2:p.Thr159Ala
ENST00000451957.2:c.275+3449A>G	ENSP00000407517.2:n.275+3449A>G
NM_000178.2:c.475A>G	NP_000169.1:p.Thr159Ala
XM_005260406.3:c.475A>G	XP_005260463.1:p.Thr159Ala
XM_011528796.1:c.475A>G	XP_011527098.1:p.Thr159Ala
NM_000178.4:c.475A>G MANE Select	NP_000169.1:p.Thr159Ala
NM_001322494.1:c.475A>G	NP_001309423.1:p.Thr159Ala
NM_001322495.1:c.475A>G	NP_001309424.1:p.Thr159Ala