Canonical Allele Identifier: CA2652574633
Gene: GSS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.34931726_34931727insTAAG , CM000682.2:g.34931726_34931727insTAAG GRCh38
NC_000020.10:g.33519529_33519530insTAAG , CM000682.1:g.33519529_33519530insTAAG GRCh37
NC_000020.9:g.32983190_32983191insTAAG NCBI36
NG_008848.1:g.29073_29074insTTAC
NG_008848.2:g.29302_29303insTTAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000642498.1:c.1029+213_1029+214insTTAC ENSP00000493631.1:n.1029+213_1029+214insTTAC
ENST00000642538.1:c.*373+213_*373+214insTTAC ENSP00000493927.1:n.*373+213_*373+214insTTAC
ENST00000643188.1:c.1029+213_1029+214insTTAC ENSP00000493903.1:n.1029+213_1029+214insTTAC
ENST00000643443.1:c.*736+213_*736+214insTTAC ENSP00000495572.1:n.*736+213_*736+214insTTAC
ENST00000643502.1:c.686+213_686+214insTTAC
ENST00000643908.1:n.1247+213_1247+214insTTAC
ENST00000644538.1:n.1306+213_1306+214insTTAC
ENST00000644793.1:c.1029+213_1029+214insTTAC ENSP00000495750.1:n.1029+213_1029+214insTTAC
ENST00000645328.1:c.407+213_407+214insTTAC
ENST00000645408.1:c.562+213_562+214insTTAC
ENST00000645723.1:n.2268+213_2268+214insTTAC
ENST00000646405.1:c.*447+213_*447+214insTTAC ENSP00000493744.1:n.*447+213_*447+214insTTAC
ENST00000646512.1:n.1175+213_1175+214insTTAC
ENST00000646735.1:c.696+213_696+214insTTAC ENSP00000493763.1:n.696+213_696+214insTTAC
ENST00000651619.1:c.1029+213_1029+214insTTAC MANE Select ENSP00000498303.1:n.1029+213_1029+214insTTAC
ENST00000216951.6:c.1029+213_1029+214insTTAC ENSP00000216951.2:n.1029+213_1029+214insTTAC
ENST00000451957.2:c.696+213_696+214insTTAC ENSP00000407517.2:n.696+213_696+214insTTAC
NM_000178.2:c.1029+213_1029+214insTTAC NP_000169.1:n.1029+213_1029+214insTTAC
XM_005260406.3:c.1029+213_1029+214insTTAC XP_005260463.1:n.1029+213_1029+214insTTAC
XM_011528796.1:c.1029+213_1029+214insTTAC XP_011527098.1:n.1029+213_1029+214insTTAC
NM_000178.4:c.1029+213_1029+214insTTAC MANE Select NP_000169.1:n.1029+213_1029+214insTTAC
NM_001322494.1:c.1029+213_1029+214insTTAC NP_001309423.1:n.1029+213_1029+214insTTAC
NM_001322495.1:c.1029+213_1029+214insTTAC NP_001309424.1:n.1029+213_1029+214insTTAC