Canonical Allele Identifier: CA408701359

Gene: GSS

Linked Data

• MyVariant Identifiers: chr20:g.33519910C>G (hg19) ; chr20:g.34932107C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34932107C>G , CM000682.2:g.34932107C>G	GRCh38
NC_000020.10:g.33519910C>G , CM000682.1:g.33519910C>G	GRCh37
NC_000020.9:g.32983571C>G	NCBI36
NG_008848.1:g.28692G>C
NG_008848.2:g.28921G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642493.1:c.*501G>C	ENSP00000493524.1:n.*501G>C
ENST00000642498.1:c.861G>C	ENSP00000493631.1:p.Glu287Asp
ENST00000642538.1:c.*205G>C	ENSP00000493927.1:n.*205G>C
ENST00000643188.1:c.861G>C	ENSP00000493903.1:p.Glu287Asp
ENST00000643443.1:c.*568G>C	ENSP00000495572.1:n.*568G>C
ENST00000643502.1:c.518G>C
ENST00000643908.1:n.1079G>C
ENST00000644538.1:n.1138G>C
ENST00000644793.1:c.861G>C	ENSP00000495750.1:p.Glu287Asp
ENST00000645328.1:c.239G>C
ENST00000645408.1:c.394G>C
ENST00000645723.1:n.2100G>C
ENST00000646405.1:c.*279G>C	ENSP00000493744.1:n.*279G>C
ENST00000646497.1:n.806G>C
ENST00000646512.1:n.1007G>C
ENST00000646735.1:c.528G>C	ENSP00000493763.1:p.Glu176Asp
ENST00000651619.1:c.861G>C MANE Select	ENSP00000498303.1:p.Glu287Asp
ENST00000216951.6:c.861G>C	ENSP00000216951.2:p.Glu287Asp
ENST00000451957.2:c.528G>C	ENSP00000407517.2:p.Glu176Asp
NM_000178.2:c.861G>C	NP_000169.1:p.Glu287Asp
XM_005260406.3:c.861G>C	XP_005260463.1:p.Glu287Asp
XM_011528796.1:c.861G>C	XP_011527098.1:p.Glu287Asp
NM_000178.4:c.861G>C MANE Select	NP_000169.1:p.Glu287Asp
NM_001322494.1:c.861G>C	NP_001309423.1:p.Glu287Asp
NM_001322495.1:c.861G>C	NP_001309424.1:p.Glu287Asp