Canonical Allele Identifier: CA415187066
Gene: SSR4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153798117C>T , CM000685.2:g.153798117C>T GRCh38
NC_000023.10:g.153063572C>T , CM000685.1:g.153063572C>T GRCh37
NC_000023.9:g.152716766C>T NCBI36
NG_041795.1:g.8943C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370086.8:c.398C>T MANE Select ENSP00000359103.3:p.Thr133Ile
ENST00000320857.7:c.398C>T ENSP00000317331.3:p.Thr133Ile
ENST00000370085.3:c.323C>T ENSP00000359102.3:p.Thr108Ile
ENST00000370086.7:c.398C>T ENSP00000359103.3:p.Thr133Ile
ENST00000370087.5:c.398C>T ENSP00000359104.1:p.Thr133Ile
ENST00000447375.1:n.238C>T
ENST00000460616.5:n.2106C>T
ENST00000471880.5:n.601C>T
ENST00000482902.5:n.2225C>T
ENST00000485612.5:n.513C>T
ENST00000486204.5:n.470C>T
NM_001204526.1:c.431C>T NP_001191455.1:p.Thr144Ile
NM_001204527.1:c.422C>T NP_001191456.1:p.Thr141Ile
NM_006280.2:c.398C>T NP_006271.1:p.Thr133Ile
NR_037927.1:n.743C>T
XM_011531186.1:c.398C>T XP_011529488.1:p.Thr133Ile
XM_011531187.1:c.398C>T XP_011529489.1:p.Thr133Ile
XM_017029756.1:c.209C>T XP_016885245.1:p.Thr70Ile
XM_017029757.1:c.209C>T XP_016885246.1:p.Thr70Ile
XM_024452428.1:c.209C>T XP_024308196.1:p.Thr70Ile
NM_001204527.2:c.422C>T NP_001191456.1:p.Thr141Ile
NM_006280.3:c.398C>T MANE Select NP_006271.1:p.Thr133Ile