Canonical Allele Identifier: CA2816224986

Gene: GSS

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34932244T>A , CM000682.2:g.34932244T>A	GRCh38
NC_000020.10:g.33520047T>A , CM000682.1:g.33520047T>A	GRCh37
NC_000020.9:g.32983708T>A	NCBI36
NG_008848.1:g.28555A>T
NG_008848.2:g.28784A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642493.1:c.*475-111A>T	ENSP00000493524.1:n.*475-111A>T
ENST00000642498.1:c.835-111A>T	ENSP00000493631.1:n.835-111A>T
ENST00000642538.1:c.*179-111A>T	ENSP00000493927.1:n.*179-111A>T
ENST00000643188.1:c.835-111A>T	ENSP00000493903.1:n.835-111A>T
ENST00000643443.1:c.*542-111A>T	ENSP00000495572.1:n.*542-111A>T
ENST00000643502.1:c.492-111A>T
ENST00000643908.1:n.1053-111A>T
ENST00000644538.1:n.1112-111A>T
ENST00000644793.1:c.835-111A>T	ENSP00000495750.1:n.835-111A>T
ENST00000645328.1:c.213-111A>T
ENST00000645408.1:c.368-111A>T
ENST00000645723.1:n.2074-111A>T
ENST00000646405.1:c.*253-111A>T	ENSP00000493744.1:n.*253-111A>T
ENST00000646497.1:n.780-111A>T
ENST00000646512.1:n.981-111A>T
ENST00000646735.1:c.502-111A>T	ENSP00000493763.1:n.502-111A>T
ENST00000651619.1:c.835-111A>T MANE Select	ENSP00000498303.1:n.835-111A>T
ENST00000216951.6:c.835-111A>T	ENSP00000216951.2:n.835-111A>T
ENST00000451957.2:c.502-111A>T	ENSP00000407517.2:n.502-111A>T
NM_000178.2:c.835-111A>T	NP_000169.1:n.835-111A>T
XM_005260406.3:c.835-111A>T	XP_005260463.1:n.835-111A>T
XM_011528796.1:c.835-111A>T	XP_011527098.1:n.835-111A>T
NM_000178.4:c.835-111A>T MANE Select	NP_000169.1:n.835-111A>T
NM_001322494.1:c.835-111A>T	NP_001309423.1:n.835-111A>T
NM_001322495.1:c.835-111A>T	NP_001309424.1:n.835-111A>T