Canonical Allele Identifier: CA2466480467

Gene: SSR4

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153797955_153797960delinsCTCCTT , CM000685.2:g.153797955_153797960delinsCTCCTT	GRCh38
NC_000023.10:g.153063410_153063415delinsCTCCTT , CM000685.1:g.153063410_153063415delinsCTCCTT	GRCh37
NC_000023.9:g.152716604_152716609delinsCTCCTT	NCBI36
NG_041795.1:g.8781_8786delinsCTCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370086.8:c.352-116_352-111delinsCTCCTT MANE Select	ENSP00000359103.3:n.352-116_352-111delinsCTCCTT
ENST00000320857.7:c.352-116_352-111delinsCTCCTT	ENSP00000317331.3:n.352-116_352-111delinsCTCCTT
ENST00000370085.3:c.277-116_277-111delinsCTCCTT	ENSP00000359102.3:n.277-116_277-111delinsCTCCTT
ENST00000370086.7:c.352-116_352-111delinsCTCCTT	ENSP00000359103.3:n.352-116_352-111delinsCTCCTT
ENST00000370087.5:c.352-116_352-111delinsCTCCTT	ENSP00000359104.1:n.352-116_352-111delinsCTCCTT
ENST00000447375.1:n.192-116_192-111delinsCTCCTT
ENST00000460616.5:n.2060-116_2060-111delinsCTCCTT
ENST00000471880.5:n.555-116_555-111delinsCTCCTT
ENST00000482902.5:n.2179-116_2179-111delinsCTCCTT
ENST00000485612.5:n.467-116_467-111delinsCTCCTT
ENST00000486204.5:n.424-116_424-111delinsCTCCTT
NM_001204526.1:c.385-116_385-111delinsCTCCTT	NP_001191455.1:n.385-116_385-111delinsCTCCTT
NM_001204527.1:c.376-116_376-111delinsCTCCTT	NP_001191456.1:n.376-116_376-111delinsCTCCTT
NM_006280.2:c.352-116_352-111delinsCTCCTT	NP_006271.1:n.352-116_352-111delinsCTCCTT
NR_037927.1:n.697-116_697-111delinsCTCCTT
XM_011531186.1:c.352-116_352-111delinsCTCCTT	XP_011529488.1:n.352-116_352-111delinsCTCCTT
XM_011531187.1:c.352-116_352-111delinsCTCCTT	XP_011529489.1:n.352-116_352-111delinsCTCCTT
XM_017029756.1:c.163-116_163-111delinsCTCCTT	XP_016885245.1:n.163-116_163-111delinsCTCCTT
XM_017029757.1:c.163-116_163-111delinsCTCCTT	XP_016885246.1:n.163-116_163-111delinsCTCCTT
XM_024452428.1:c.163-116_163-111delinsCTCCTT	XP_024308196.1:n.163-116_163-111delinsCTCCTT
NM_001204527.2:c.376-116_376-111delinsCTCCTT	NP_001191456.1:n.376-116_376-111delinsCTCCTT
NM_006280.3:c.352-116_352-111delinsCTCCTT MANE Select	NP_006271.1:n.352-116_352-111delinsCTCCTT