Canonical Allele Identifier: CA2816224954

Gene: GSS

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34931837_34931838del , CM000682.2:g.34931837_34931838del	GRCh38
NC_000020.10:g.33519640_33519641del , CM000682.1:g.33519640_33519641del	GRCh37
NC_000020.9:g.32983301_32983302del	NCBI36
NG_008848.1:g.28961_28962del
NG_008848.2:g.29190_29191del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642498.1:c.1029+101_1029+102del	ENSP00000493631.1:n.1029+101_1029+102del
ENST00000642538.1:c.*373+101_*373+102del	ENSP00000493927.1:n.*373+101_*373+102del
ENST00000643188.1:c.1029+101_1029+102del	ENSP00000493903.1:n.1029+101_1029+102del
ENST00000643443.1:c.*736+101_*736+102del	ENSP00000495572.1:n.*736+101_*736+102del
ENST00000643502.1:c.686+101_686+102del
ENST00000643908.1:n.1247+101_1247+102del
ENST00000644538.1:n.1306+101_1306+102del
ENST00000644793.1:c.1029+101_1029+102del	ENSP00000495750.1:n.1029+101_1029+102del
ENST00000645328.1:c.407+101_407+102del
ENST00000645408.1:c.562+101_562+102del
ENST00000645723.1:n.2268+101_2268+102del
ENST00000646405.1:c.*447+101_*447+102del	ENSP00000493744.1:n.*447+101_*447+102del
ENST00000646512.1:n.1175+101_1175+102del
ENST00000646735.1:c.696+101_696+102del	ENSP00000493763.1:n.696+101_696+102del
ENST00000651619.1:c.1029+101_1029+102del MANE Select	ENSP00000498303.1:n.1029+101_1029+102del
ENST00000216951.6:c.1029+101_1029+102del	ENSP00000216951.2:n.1029+101_1029+102del
ENST00000451957.2:c.696+101_696+102del	ENSP00000407517.2:n.696+101_696+102del
NM_000178.2:c.1029+101_1029+102del	NP_000169.1:n.1029+101_1029+102del
XM_005260406.3:c.1029+101_1029+102del	XP_005260463.1:n.1029+101_1029+102del
XM_011528796.1:c.1029+101_1029+102del	XP_011527098.1:n.1029+101_1029+102del
NM_000178.4:c.1029+101_1029+102del MANE Select	NP_000169.1:n.1029+101_1029+102del
NM_001322494.1:c.1029+101_1029+102del	NP_001309423.1:n.1029+101_1029+102del
NM_001322495.1:c.1029+101_1029+102del	NP_001309424.1:n.1029+101_1029+102del