Canonical Allele Identifier: CA408700085

Gene: GSS

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34928952C>T , CM000682.2:g.34928952C>T	GRCh38
NC_000020.10:g.33516755C>T , CM000682.1:g.33516755C>T	GRCh37
NC_000020.9:g.32980416C>T	NCBI36
NG_008848.1:g.31847G>A
NG_011520.1:g.59011C>T
NG_008848.2:g.32076G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642498.1:c.*234G>A	ENSP00000493631.1:n.*234G>A
ENST00000643188.1:c.1302-1G>A	ENSP00000493903.1:n.1302-1G>A
ENST00000643443.1:c.*1009-1G>A	ENSP00000495572.1:n.*1009-1G>A
ENST00000643502.1:c.959-1G>A
ENST00000643908.1:n.1520-1G>A
ENST00000644538.1:n.1579-1G>A
ENST00000644793.1:c.1302-1G>A	ENSP00000495750.1:n.1302-1G>A
ENST00000645328.1:c.490-1G>A
ENST00000645723.1:n.2541-1G>A
ENST00000646405.1:c.*720-1G>A	ENSP00000493744.1:n.*720-1G>A
ENST00000646512.1:n.1448-1G>A
ENST00000646735.1:c.969-1G>A	ENSP00000493763.1:n.969-1G>A
ENST00000651619.1:c.1302-1G>A MANE Select	ENSP00000498303.1:n.1302-1G>A
ENST00000216951.6:c.1302-1G>A	ENSP00000216951.2:n.1302-1G>A
ENST00000451957.2:c.969-1G>A	ENSP00000407517.2:n.969-1G>A
NM_000178.2:c.1302-1G>A	NP_000169.1:n.1302-1G>A
XM_005260406.3:c.1302-1G>A	XP_005260463.1:n.1302-1G>A
XM_011528796.1:c.1302-1G>A	XP_011527098.1:n.1302-1G>A
NM_000178.4:c.1302-1G>A MANE Select	NP_000169.1:n.1302-1G>A
NM_001322494.1:c.1302-1G>A	NP_001309423.1:n.1302-1G>A
NM_001322495.1:c.1302-1G>A	NP_001309424.1:n.1302-1G>A