Canonical Allele Identifier: CA2361424287
Gene: GSS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.34935249_34935250delinsGA , CM000682.2:g.34935249_34935250delinsGA GRCh38
NC_000020.10:g.33523052_33523053delinsGA , CM000682.1:g.33523052_33523053delinsGA GRCh37
NC_000020.9:g.32986713_32986714delinsGA NCBI36
NG_008848.1:g.25549_25550delinsTC
NG_008848.2:g.25778_25779delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000642493.1:c.*474+1513_*474+1514delinsTC ENSP00000493524.1:n.*474+1513_*474+1514delinsTC
ENST00000642498.1:c.834+326_834+327delinsTC ENSP00000493631.1:n.834+326_834+327delinsTC
ENST00000642538.1:c.*178+326_*178+327delinsTC ENSP00000493927.1:n.*178+326_*178+327delinsTC
ENST00000643188.1:c.834+326_834+327delinsTC ENSP00000493903.1:n.834+326_834+327delinsTC
ENST00000643443.1:c.*541+326_*541+327delinsTC ENSP00000495572.1:n.*541+326_*541+327delinsTC
ENST00000643502.1:c.491+326_491+327delinsTC
ENST00000643908.1:n.1052+1693_1052+1694delinsTC
ENST00000644538.1:n.1111+326_1111+327delinsTC
ENST00000644793.1:c.834+326_834+327delinsTC ENSP00000495750.1:n.834+326_834+327delinsTC
ENST00000645328.1:c.212+326_212+327delinsTC
ENST00000645408.1:c.367+1513_367+1514delinsTC
ENST00000645723.1:n.2073+326_2073+327delinsTC
ENST00000646405.1:c.*252+1513_*252+1514delinsTC ENSP00000493744.1:n.*252+1513_*252+1514delinsTC
ENST00000646497.1:n.779+326_779+327delinsTC
ENST00000646502.1:n.1316+326_1316+327delinsTC
ENST00000646512.1:n.980+1513_980+1514delinsTC
ENST00000646735.1:c.501+326_501+327delinsTC ENSP00000493763.1:n.501+326_501+327delinsTC
ENST00000651619.1:c.834+326_834+327delinsTC MANE Select ENSP00000498303.1:n.834+326_834+327delinsTC
ENST00000216951.6:c.834+326_834+327delinsTC ENSP00000216951.2:n.834+326_834+327delinsTC
ENST00000451957.2:c.501+326_501+327delinsTC ENSP00000407517.2:n.501+326_501+327delinsTC
NM_000178.2:c.834+326_834+327delinsTC NP_000169.1:n.834+326_834+327delinsTC
XM_005260406.3:c.834+326_834+327delinsTC XP_005260463.1:n.834+326_834+327delinsTC
XM_011528796.1:c.834+326_834+327delinsTC XP_011527098.1:n.834+326_834+327delinsTC
NM_000178.4:c.834+326_834+327delinsTC MANE Select NP_000169.1:n.834+326_834+327delinsTC
NM_001322494.1:c.834+326_834+327delinsTC NP_001309423.1:n.834+326_834+327delinsTC
NM_001322495.1:c.834+326_834+327delinsTC NP_001309424.1:n.834+326_834+327delinsTC