Canonical Allele Identifier: CA2466480529
Gene: SSR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153798044_153798055delinsAGCACCTCCCTT , CM000685.2:g.153798044_153798055delinsAGCACCTCCCTT GRCh38
NC_000023.10:g.153063499_153063510delinsAGCACCTCCCTT , CM000685.1:g.153063499_153063510delinsAGCACCTCCCTT GRCh37
NC_000023.9:g.152716693_152716704delinsAGCACCTCCCTT NCBI36
NG_041795.1:g.8870_8881delinsAGCACCTCCCTT

Transcript Alleles

HGVS Amino-acid change
ENST00000370086.8:c.352-27_352-16delinsAGCACCTCCCTT MANE Select ENSP00000359103.3:n.352-27_352-16delinsAG...
ENST00000320857.7:c.352-27_352-16delinsAGCACCTCCCTT ENSP00000317331.3:n.352-27_352-16delinsAG...
ENST00000370085.3:c.277-27_277-16delinsAGCACCTCCCTT ENSP00000359102.3:n.277-27_277-16delinsAG...
ENST00000370086.7:c.352-27_352-16delinsAGCACCTCCCTT ENSP00000359103.3:n.352-27_352-16delinsAG...
ENST00000370087.5:c.352-27_352-16delinsAGCACCTCCCTT ENSP00000359104.1:n.352-27_352-16delinsAG...
ENST00000447375.1:n.192-27_192-16delinsAGCACCTCCCTT
ENST00000460616.5:n.2060-27_2060-16delinsAGCACCTCCCTT
ENST00000471880.5:n.555-27_555-16delinsAGCACCTCCCTT
ENST00000482902.5:n.2179-27_2179-16delinsAGCACCTCCCTT
ENST00000485612.5:n.467-27_467-16delinsAGCACCTCCCTT
ENST00000486204.5:n.424-27_424-16delinsAGCACCTCCCTT
NM_001204526.1:c.385-27_385-16delinsAGCACCTCCCTT NP_001191455.1:n.385-27_385-16delinsAGCAC...
NM_001204527.1:c.376-27_376-16delinsAGCACCTCCCTT NP_001191456.1:n.376-27_376-16delinsAGCAC...
NM_006280.2:c.352-27_352-16delinsAGCACCTCCCTT NP_006271.1:n.352-27_352-16delinsAGCACCTC...
NR_037927.1:n.697-27_697-16delinsAGCACCTCCCTT
XM_011531186.1:c.352-27_352-16delinsAGCACCTCCCTT XP_011529488.1:n.352-27_352-16delinsAGCAC...
XM_011531187.1:c.352-27_352-16delinsAGCACCTCCCTT XP_011529489.1:n.352-27_352-16delinsAGCAC...
XM_017029756.1:c.163-27_163-16delinsAGCACCTCCCTT XP_016885245.1:n.163-27_163-16delinsAGCAC...
XM_017029757.1:c.163-27_163-16delinsAGCACCTCCCTT XP_016885246.1:n.163-27_163-16delinsAGCAC...
XM_024452428.1:c.163-27_163-16delinsAGCACCTCCCTT XP_024308196.1:n.163-27_163-16delinsAGCAC...
NM_001204527.2:c.376-27_376-16delinsAGCACCTCCCTT NP_001191456.1:n.376-27_376-16delinsAGCAC...
NM_006280.3:c.352-27_352-16delinsAGCACCTCCCTT MANE Select NP_006271.1:n.352-27_352-16delinsAGCACCTC...