Canonical Allele Identifier: CA2466480537
Gene: SSR4 HGNC NCBI

Linked Data

dbSNP Id: rs2092153240

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153798054_153798055del , CM000685.2:g.153798054_153798055del GRCh38
NC_000023.10:g.153063509_153063510del , CM000685.1:g.153063509_153063510del GRCh37
NC_000023.9:g.152716703_152716704del NCBI36
NG_041795.1:g.8880_8881del

Transcript Alleles

HGVS Amino-acid Change
ENST00000370086.8:c.352-17_352-16del MANE Select ENSP00000359103.3:n.352-17_352-16del
ENST00000320857.7:c.352-17_352-16del ENSP00000317331.3:n.352-17_352-16del
ENST00000370085.3:c.277-17_277-16del ENSP00000359102.3:n.277-17_277-16del
ENST00000370086.7:c.352-17_352-16del ENSP00000359103.3:n.352-17_352-16del
ENST00000370087.5:c.352-17_352-16del ENSP00000359104.1:n.352-17_352-16del
ENST00000447375.1:n.192-17_192-16del
ENST00000460616.5:n.2060-17_2060-16del
ENST00000471880.5:n.555-17_555-16del
ENST00000482902.5:n.2179-17_2179-16del
ENST00000485612.5:n.467-17_467-16del
ENST00000486204.5:n.424-17_424-16del
NM_001204526.1:c.385-17_385-16del NP_001191455.1:n.385-17_385-16del
NM_001204527.1:c.376-17_376-16del NP_001191456.1:n.376-17_376-16del
NM_006280.2:c.352-17_352-16del NP_006271.1:n.352-17_352-16del
NR_037927.1:n.697-17_697-16del
XM_011531186.1:c.352-17_352-16del XP_011529488.1:n.352-17_352-16del
XM_011531187.1:c.352-17_352-16del XP_011529489.1:n.352-17_352-16del
XM_017029756.1:c.163-17_163-16del XP_016885245.1:n.163-17_163-16del
XM_017029757.1:c.163-17_163-16del XP_016885246.1:n.163-17_163-16del
XM_024452428.1:c.163-17_163-16del XP_024308196.1:n.163-17_163-16del
NM_001204527.2:c.376-17_376-16del NP_001191456.1:n.376-17_376-16del
NM_006280.3:c.352-17_352-16del MANE Select NP_006271.1:n.352-17_352-16del