Canonical Allele Identifier: CA2816224955

Gene: GSS

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34931842_34931847del , CM000682.2:g.34931842_34931847del	GRCh38
NC_000020.10:g.33519645_33519650del , CM000682.1:g.33519645_33519650del	GRCh37
NC_000020.9:g.32983306_32983311del	NCBI36
NG_008848.1:g.28953_28958del
NG_008848.2:g.29182_29187del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642498.1:c.1029+93_1029+98del	ENSP00000493631.1:n.1029+93_1029+98del
ENST00000642538.1:c.*373+93_*373+98del	ENSP00000493927.1:n.*373+93_*373+98del
ENST00000643188.1:c.1029+93_1029+98del	ENSP00000493903.1:n.1029+93_1029+98del
ENST00000643443.1:c.*736+93_*736+98del	ENSP00000495572.1:n.*736+93_*736+98del
ENST00000643502.1:c.686+93_686+98del
ENST00000643908.1:n.1247+93_1247+98del
ENST00000644538.1:n.1306+93_1306+98del
ENST00000644793.1:c.1029+93_1029+98del	ENSP00000495750.1:n.1029+93_1029+98del
ENST00000645328.1:c.407+93_407+98del
ENST00000645408.1:c.562+93_562+98del
ENST00000645723.1:n.2268+93_2268+98del
ENST00000646405.1:c.*447+93_*447+98del	ENSP00000493744.1:n.*447+93_*447+98del
ENST00000646512.1:n.1175+93_1175+98del
ENST00000646735.1:c.696+93_696+98del	ENSP00000493763.1:n.696+93_696+98del
ENST00000651619.1:c.1029+93_1029+98del MANE Select	ENSP00000498303.1:n.1029+93_1029+98del
ENST00000216951.6:c.1029+93_1029+98del	ENSP00000216951.2:n.1029+93_1029+98del
ENST00000451957.2:c.696+93_696+98del	ENSP00000407517.2:n.696+93_696+98del
NM_000178.2:c.1029+93_1029+98del	NP_000169.1:n.1029+93_1029+98del
XM_005260406.3:c.1029+93_1029+98del	XP_005260463.1:n.1029+93_1029+98del
XM_011528796.1:c.1029+93_1029+98del	XP_011527098.1:n.1029+93_1029+98del
NM_000178.4:c.1029+93_1029+98del MANE Select	NP_000169.1:n.1029+93_1029+98del
NM_001322494.1:c.1029+93_1029+98del	NP_001309423.1:n.1029+93_1029+98del
NM_001322495.1:c.1029+93_1029+98del	NP_001309424.1:n.1029+93_1029+98del