Canonical Allele Identifier: CA2652574657

Gene: GSS

Linked Data

• gnomAD v4: 20-34931814-TCAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34931817_34931819del , CM000682.2:g.34931817_34931819del	GRCh38
NC_000020.10:g.33519620_33519622del , CM000682.1:g.33519620_33519622del	GRCh37
NC_000020.9:g.32983281_32983283del	NCBI36
NG_008848.1:g.28982_28984del
NG_008848.2:g.29211_29213del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642498.1:c.1029+122_1029+124del	ENSP00000493631.1:n.1029+122_1029+124del
ENST00000642538.1:c.*373+122_*373+124del	ENSP00000493927.1:n.*373+122_*373+124del
ENST00000643188.1:c.1029+122_1029+124del	ENSP00000493903.1:n.1029+122_1029+124del
ENST00000643443.1:c.*736+122_*736+124del	ENSP00000495572.1:n.*736+122_*736+124del
ENST00000643502.1:c.686+122_686+124del
ENST00000643908.1:n.1247+122_1247+124del
ENST00000644538.1:n.1306+122_1306+124del
ENST00000644793.1:c.1029+122_1029+124del	ENSP00000495750.1:n.1029+122_1029+124del
ENST00000645328.1:c.407+122_407+124del
ENST00000645408.1:c.562+122_562+124del
ENST00000645723.1:n.2268+122_2268+124del
ENST00000646405.1:c.*447+122_*447+124del	ENSP00000493744.1:n.*447+122_*447+124del
ENST00000646512.1:n.1175+122_1175+124del
ENST00000646735.1:c.696+122_696+124del	ENSP00000493763.1:n.696+122_696+124del
ENST00000651619.1:c.1029+122_1029+124del MANE Select	ENSP00000498303.1:n.1029+122_1029+124del
ENST00000216951.6:c.1029+122_1029+124del	ENSP00000216951.2:n.1029+122_1029+124del
ENST00000451957.2:c.696+122_696+124del	ENSP00000407517.2:n.696+122_696+124del
NM_000178.2:c.1029+122_1029+124del	NP_000169.1:n.1029+122_1029+124del
XM_005260406.3:c.1029+122_1029+124del	XP_005260463.1:n.1029+122_1029+124del
XM_011528796.1:c.1029+122_1029+124del	XP_011527098.1:n.1029+122_1029+124del
NM_000178.4:c.1029+122_1029+124del MANE Select	NP_000169.1:n.1029+122_1029+124del
NM_001322494.1:c.1029+122_1029+124del	NP_001309423.1:n.1029+122_1029+124del
NM_001322495.1:c.1029+122_1029+124del	NP_001309424.1:n.1029+122_1029+124del