Canonical Allele Identifier: CA2695065519
Gene: SSR4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153798004_153798005insCACCC , CM000685.2:g.153798004_153798005insCACCC GRCh38
NC_000023.10:g.153063459_153063460insCACCC , CM000685.1:g.153063459_153063460insCACCC GRCh37
NC_000023.9:g.152716653_152716654insCACCC NCBI36
NG_041795.1:g.8830_8831insCACCC

Transcript Alleles

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