Canonical Allele Identifier: CA2602662305
Gene: SSR4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153798028_153798030del , CM000685.2:g.153798028_153798030del GRCh38
NC_000023.10:g.153063483_153063485del , CM000685.1:g.153063483_153063485del GRCh37
NC_000023.9:g.152716677_152716679del NCBI36
NG_041795.1:g.8854_8856del

Transcript Alleles

HGVS Amino-acid Change
ENST00000370086.8:c.352-43_352-41del MANE Select ENSP00000359103.3:n.352-43_352-41del
ENST00000320857.7:c.352-43_352-41del ENSP00000317331.3:n.352-43_352-41del
ENST00000370085.3:c.277-43_277-41del ENSP00000359102.3:n.277-43_277-41del
ENST00000370086.7:c.352-43_352-41del ENSP00000359103.3:n.352-43_352-41del
ENST00000370087.5:c.352-43_352-41del ENSP00000359104.1:n.352-43_352-41del
ENST00000447375.1:n.192-43_192-41del
ENST00000460616.5:n.2060-43_2060-41del
ENST00000471880.5:n.555-43_555-41del
ENST00000482902.5:n.2179-43_2179-41del
ENST00000485612.5:n.467-43_467-41del
ENST00000486204.5:n.424-43_424-41del
NM_001204526.1:c.385-43_385-41del NP_001191455.1:n.385-43_385-41del
NM_001204527.1:c.376-43_376-41del NP_001191456.1:n.376-43_376-41del
NM_006280.2:c.352-43_352-41del NP_006271.1:n.352-43_352-41del
NR_037927.1:n.697-43_697-41del
XM_011531186.1:c.352-43_352-41del XP_011529488.1:n.352-43_352-41del
XM_011531187.1:c.352-43_352-41del XP_011529489.1:n.352-43_352-41del
XM_017029756.1:c.163-43_163-41del XP_016885245.1:n.163-43_163-41del
XM_017029757.1:c.163-43_163-41del XP_016885246.1:n.163-43_163-41del
XM_024452428.1:c.163-43_163-41del XP_024308196.1:n.163-43_163-41del
NM_001204527.2:c.376-43_376-41del NP_001191456.1:n.376-43_376-41del
NM_006280.3:c.352-43_352-41del MANE Select NP_006271.1:n.352-43_352-41del