Canonical Allele Identifier: CA2638377599
Gene: KANSL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46067642del , CM000679.2:g.46067642del GRCh38
NC_000017.9:g.41500830del NCBI36
NG_032784.1:g.162736del

Transcript Alleles

HGVS Amino-acid Change
ENST00000432791.7:c.1562del MANE Select ENSP00000387393.3:p.Asn521ThrfsTer?
ENST00000571698.2:c.1562del ENSP00000459330.2:p.Asn521ThrfsTer?
ENST00000572904.6:c.1562del ENSP00000461484.1:p.Asn521ThrfsTer?
ENST00000574590.6:c.1562del ENSP00000461812.2:p.Asn521ThrfsTer?
ENST00000575318.6:c.1562del ENSP00000461299.1:p.Asn521ThrfsTer?
ENST00000577114.2:n.288del
ENST00000638275.1:c.1562del ENSP00000492576.1:p.Asn521ThrfsTer?
ENST00000639150.1:c.296del ENSP00000491906.1:p.Asn99ThrfsTer?
ENST00000639375.1:n.1800del
ENST00000639531.1:c.1562del ENSP00000491765.1:p.Asn521ThrfsTer?
ENST00000639853.1:c.733del
ENST00000648792.1:c.1562del ENSP00000497628.1:p.Asn521ThrfsTer?
ENST00000262419.10:c.1562del ENSP00000262419.6:p.Asn521ThrfsTer?
ENST00000432791.5:c.1562del ENSP00000387393.2:p.Asn521ThrfsTer?
ENST00000572904.5:c.1562del ENSP00000461484.1:p.Asn521ThrfsTer?
ENST00000574590.5:c.1562del ENSP00000461812.1:p.Asn521ThrfsTer?
ENST00000575318.5:c.1562del ENSP00000461299.1:p.Asn521ThrfsTer?
ENST00000577114.1:n.359del
NM_001193465.1:c.1562del NP_001180394.1:p.Asn521ThrfsTer?
NM_001193466.1:c.1562del NP_001180395.1:p.Asn521ThrfsTer?
NM_015443.3:c.1562del NP_056258.1:p.Asn521ThrfsTer?
XM_006721823.1:c.1562del XP_006721886.1:p.Asn521ThrfsTer?
XM_006721824.2:c.1562del XP_006721887.1:p.Asn521ThrfsTer?
XM_011524628.1:c.1562del XP_011522930.1:p.Asn521ThrfsTer?
XM_011524629.1:c.1460del XP_011522931.1:p.Asn487ThrfsTer?
XM_011524630.1:c.1562del XP_011522932.1:p.Asn521ThrfsTer?
XM_011524631.1:c.1562del XP_011522933.1:p.Asn521ThrfsTer?
XM_011524632.1:c.332del XP_011522934.1:p.Asn111ThrfsTer?
XM_006721823.2:c.1562del XP_006721886.1:p.Asn521ThrfsTer?
XM_006721824.4:c.1562del XP_006721887.1:p.Asn521ThrfsTer?
XM_011524628.3:c.1562del XP_011522930.1:p.Asn521ThrfsTer?
XM_011524629.3:c.1460del XP_011522931.1:p.Asn487ThrfsTer?
XM_011524630.3:c.1562del XP_011522932.1:p.Asn521ThrfsTer?
XM_011524631.3:c.1562del XP_011522933.1:p.Asn521ThrfsTer?
XM_011524632.3:c.332del XP_011522934.1:p.Asn111ThrfsTer?
XM_017024488.2:c.1562del XP_016879977.1:p.Asn521ThrfsTer?
XM_017024489.1:c.1460del XP_016879978.1:p.Asn487ThrfsTer?
NM_001193466.2:c.1562del NP_001180395.1:p.Asn521ThrfsTer?
NM_015443.4:c.1562del MANE Select NP_056258.1:p.Asn521ThrfsTer?
NM_001193465.2:c.1562del NP_001180394.1:p.Asn521ThrfsTer?
NM_001379198.1:c.1562del NP_001366127.1:p.Asn521ThrfsTer?