Canonical Allele Identifier: CA415187078
Gene: SSR4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153798122A>T , CM000685.2:g.153798122A>T GRCh38
NC_000023.10:g.153063577A>T , CM000685.1:g.153063577A>T GRCh37
NC_000023.9:g.152716771A>T NCBI36
NG_041795.1:g.8948A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370086.8:c.403A>T MANE Select ENSP00000359103.3:p.Ser135Cys
ENST00000320857.7:c.403A>T ENSP00000317331.3:p.Ser135Cys
ENST00000370085.3:c.328A>T ENSP00000359102.3:p.Ser110Cys
ENST00000370086.7:c.403A>T ENSP00000359103.3:p.Ser135Cys
ENST00000370087.5:c.403A>T ENSP00000359104.1:p.Ser135Cys
ENST00000447375.1:n.243A>T
ENST00000460616.5:n.2111A>T
ENST00000471880.5:n.606A>T
ENST00000482902.5:n.2230A>T
ENST00000485612.5:n.518A>T
ENST00000486204.5:n.475A>T
NM_001204526.1:c.436A>T NP_001191455.1:p.Ser146Cys
NM_001204527.1:c.427A>T NP_001191456.1:p.Ser143Cys
NM_006280.2:c.403A>T NP_006271.1:p.Ser135Cys
NR_037927.1:n.748A>T
XM_011531186.1:c.403A>T XP_011529488.1:p.Ser135Cys
XM_011531187.1:c.403A>T XP_011529489.1:p.Ser135Cys
XM_017029756.1:c.214A>T XP_016885245.1:p.Ser72Cys
XM_017029757.1:c.214A>T XP_016885246.1:p.Ser72Cys
XM_024452428.1:c.214A>T XP_024308196.1:p.Ser72Cys
NM_001204527.2:c.427A>T NP_001191456.1:p.Ser143Cys
NM_006280.3:c.403A>T MANE Select NP_006271.1:p.Ser135Cys