Canonical Allele Identifier: CA408702408

Gene: GSS

Linked Data

• MyVariant Identifiers: chr20:g.33523436C>G (hg19) ; chr20:g.34935633C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34935633C>G , CM000682.2:g.34935633C>G	GRCh38
NC_000020.10:g.33523436C>G , CM000682.1:g.33523436C>G	GRCh37
NC_000020.9:g.32987097C>G	NCBI36
NG_008848.1:g.25166G>C
NG_008848.2:g.25395G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642493.1:c.*474+1130G>C	ENSP00000493524.1:n.*474+1130G>C
ENST00000642498.1:c.777G>C	ENSP00000493631.1:p.Gln259His
ENST00000642538.1:c.*121G>C	ENSP00000493927.1:n.*121G>C
ENST00000643188.1:c.777G>C	ENSP00000493903.1:p.Gln259His
ENST00000643443.1:c.*484G>C	ENSP00000495572.1:n.*484G>C
ENST00000643502.1:c.434G>C
ENST00000643908.1:n.1052+1310G>C
ENST00000644538.1:n.1054G>C
ENST00000644793.1:c.777G>C	ENSP00000495750.1:p.Gln259His
ENST00000645328.1:c.155G>C
ENST00000645408.1:c.367+1130G>C
ENST00000645723.1:n.2016G>C
ENST00000646405.1:c.*252+1130G>C	ENSP00000493744.1:n.*252+1130G>C
ENST00000646497.1:n.722G>C
ENST00000646502.1:n.1259G>C
ENST00000646512.1:n.980+1130G>C
ENST00000646735.1:c.444G>C	ENSP00000493763.1:p.Gln148His
ENST00000646766.1:c.*407G>C	ENSP00000494333.1:n.*407G>C
ENST00000651619.1:c.777G>C MANE Select	ENSP00000498303.1:p.Gln259His
ENST00000216951.6:c.777G>C	ENSP00000216951.2:p.Gln259His
ENST00000451957.2:c.444G>C	ENSP00000407517.2:p.Gln148His
NM_000178.2:c.777G>C	NP_000169.1:p.Gln259His
XM_005260406.3:c.777G>C	XP_005260463.1:p.Gln259His
XM_011528796.1:c.777G>C	XP_011527098.1:p.Gln259His
NM_000178.4:c.777G>C MANE Select	NP_000169.1:p.Gln259His
NM_001322494.1:c.777G>C	NP_001309423.1:p.Gln259His
NM_001322495.1:c.777G>C	NP_001309424.1:p.Gln259His