Canonical Allele Identifier: CA2695065512
Gene: SSR4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153798004_153798005insCCCCCC , CM000685.2:g.153798004_153798005insCCCCCC GRCh38
NC_000023.10:g.153063459_153063460insCCCCCC , CM000685.1:g.153063459_153063460insCCCCCC GRCh37
NC_000023.9:g.152716653_152716654insCCCCCC NCBI36
NG_041795.1:g.8830_8831insCCCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000370086.8:c.352-67_352-66insCCCCCC MANE Select ENSP00000359103.3:n.352-67_352-66insCCCCCC
ENST00000320857.7:c.352-67_352-66insCCCCCC ENSP00000317331.3:n.352-67_352-66insCCCCCC
ENST00000370085.3:c.277-67_277-66insCCCCCC ENSP00000359102.3:n.277-67_277-66insCCCCCC
ENST00000370086.7:c.352-67_352-66insCCCCCC ENSP00000359103.3:n.352-67_352-66insCCCCCC
ENST00000370087.5:c.352-67_352-66insCCCCCC ENSP00000359104.1:n.352-67_352-66insCCCCCC
ENST00000447375.1:n.192-67_192-66insCCCCCC
ENST00000460616.5:n.2060-67_2060-66insCCCCCC
ENST00000471880.5:n.555-67_555-66insCCCCCC
ENST00000482902.5:n.2179-67_2179-66insCCCCCC
ENST00000485612.5:n.467-67_467-66insCCCCCC
ENST00000486204.5:n.424-67_424-66insCCCCCC
NM_001204526.1:c.385-67_385-66insCCCCCC NP_001191455.1:n.385-67_385-66insCCCCCC
NM_001204527.1:c.376-67_376-66insCCCCCC NP_001191456.1:n.376-67_376-66insCCCCCC
NM_006280.2:c.352-67_352-66insCCCCCC NP_006271.1:n.352-67_352-66insCCCCCC
NR_037927.1:n.697-67_697-66insCCCCCC
XM_011531186.1:c.352-67_352-66insCCCCCC XP_011529488.1:n.352-67_352-66insCCCCCC
XM_011531187.1:c.352-67_352-66insCCCCCC XP_011529489.1:n.352-67_352-66insCCCCCC
XM_017029756.1:c.163-67_163-66insCCCCCC XP_016885245.1:n.163-67_163-66insCCCCCC
XM_017029757.1:c.163-67_163-66insCCCCCC XP_016885246.1:n.163-67_163-66insCCCCCC
XM_024452428.1:c.163-67_163-66insCCCCCC XP_024308196.1:n.163-67_163-66insCCCCCC
NM_001204527.2:c.376-67_376-66insCCCCCC NP_001191456.1:n.376-67_376-66insCCCCCC
NM_006280.3:c.352-67_352-66insCCCCCC MANE Select NP_006271.1:n.352-67_352-66insCCCCCC