Canonical Allele Identifier: CA408702361

Gene: GSS

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34935623C>T , CM000682.2:g.34935623C>T	GRCh38
NC_000020.10:g.33523426C>T , CM000682.1:g.33523426C>T	GRCh37
NC_000020.9:g.32987087C>T	NCBI36
NG_008848.1:g.25176G>A
NG_008848.2:g.25405G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000178.4:c.787G>A MANE Select	NP_000169.1:p.Val263Met
ENST00000651619.1:c.787G>A MANE Select	ENSP00000498303.1:p.Val263Met
NM_000178.2:c.787G>A	NP_000169.1:p.Val263Met
NM_001322494.1:c.787G>A	NP_001309423.1:p.Val263Met
NM_001322495.1:c.787G>A	NP_001309424.1:p.Val263Met
ENST00000216951.6:c.787G>A	ENSP00000216951.2:p.Val263Met
ENST00000451957.2:c.454G>A	ENSP00000407517.2:p.Val152Met
ENST00000642493.1:c.*474+1140G>A	ENSP00000493524.1:n.*474+1140G>A
ENST00000642498.1:c.787G>A	ENSP00000493631.1:p.Val263Met
ENST00000642538.1:c.*131G>A	ENSP00000493927.1:n.*131G>A
ENST00000643188.1:c.787G>A	ENSP00000493903.1:p.Val263Met
ENST00000643443.1:c.*494G>A	ENSP00000495572.1:n.*494G>A
ENST00000643502.1:c.444G>A
ENST00000643908.1:n.1052+1320G>A
ENST00000644538.1:n.1064G>A
ENST00000644793.1:c.787G>A	ENSP00000495750.1:p.Val263Met
ENST00000645328.1:c.165G>A
ENST00000645408.1:c.367+1140G>A
ENST00000645723.1:n.2026G>A
ENST00000646405.1:c.*252+1140G>A	ENSP00000493744.1:n.*252+1140G>A
ENST00000646497.1:n.732G>A
ENST00000646502.1:n.1269G>A
ENST00000646512.1:n.980+1140G>A
ENST00000646735.1:c.454G>A	ENSP00000493763.1:p.Val152Met
ENST00000646766.1:c.*417G>A	ENSP00000494333.1:n.*417G>A
XM_005260406.3:c.787G>A	XP_005260463.1:p.Val263Met
XM_011528796.1:c.787G>A	XP_011527098.1:p.Val263Met