Canonical Allele Identifier: CA10645979
Gene: KANSL1 HGNC NCBI

Linked Data

dbSNP Id: rs143625699

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46192799_46192801del , CM000679.2:g.46192799_46192801del GRCh38
NC_000017.10:g.44270165_44270167del , CM000679.1:g.44270165_44270167del GRCh37
NC_000017.9:g.41625942_41625944del NCBI36
NG_032784.1:g.37585_37587del

Transcript Alleles

HGVS Amino-acid change
ENST00000432791.7:c.-90+33_-90+35del MANE Select ENSP00000387393.3:n.-90+33_-90+35del
ENST00000571698.2:c.-90+960_-90+962del ENSP00000459330.2:n.-90+960_-90+962del
ENST00000572904.6:c.-89-20558_-89-20556del ENSP00000461484.1:n.-89-20558_-89-20556de...
ENST00000574590.6:c.-89-20558_-89-20556del ENSP00000461812.2:n.-89-20558_-89-20556de...
ENST00000574655.6:n.166-20558_166-20556del
ENST00000575318.6:c.-89-20558_-89-20556del ENSP00000461299.1:n.-89-20558_-89-20556de...
ENST00000576739.2:c.-89-20558_-89-20556del ENSP00000459627.1:n.-89-20558_-89-20556de...
ENST00000638269.1:n.156-20558_156-20556del
ENST00000638275.1:c.-90+33_-90+35del ENSP00000492576.1:n.-90+33_-90+35del
ENST00000638902.1:n.16-20558_16-20556del
ENST00000639099.1:n.162-20558_162-20556del
ENST00000639150.1:c.23+30881_23+30883del ENSP00000491906.1:n.23+30881_23+30883del
ENST00000639356.1:n.162-20558_162-20556del
ENST00000639375.1:n.150-20558_150-20556del
ENST00000648792.1:c.-89-20558_-89-20556del ENSP00000497628.1:n.-89-20558_-89-20556de...
ENST00000432791.5:c.-89-20558_-89-20556del ENSP00000387393.2:n.-89-20558_-89-20556de...
ENST00000571698.1:c.-90+960_-90+962del ENSP00000459330.1:n.-90+960_-90+962del
ENST00000572904.5:c.-90+33_-90+35del ENSP00000461484.1:n.-90+33_-90+35del
ENST00000574590.5:c.-89-20558_-89-20556del ENSP00000461812.1:n.-89-20558_-89-20556de...
ENST00000574655.5:c.-89-20558_-89-20556del ENSP00000459359.1:n.-89-20558_-89-20556de...
ENST00000576739.1:c.-89-20558_-89-20556del ENSP00000459627.1:n.-89-20558_-89-20556de...
NM_001193465.1:c.-89-20558_-89-20556del NP_001180394.1:n.-89-20558_-89-20556del
NM_015443.3:c.-90+33_-90+35del NP_056258.1:n.-90+33_-90+35del
XM_006721823.1:c.-89-20558_-89-20556del XP_006721886.1:n.-89-20558_-89-20556del
XM_006721824.2:c.-89-20558_-89-20556del XP_006721887.1:n.-89-20558_-89-20556del
XM_011524628.1:c.-89-20558_-89-20556del XP_011522930.1:n.-89-20558_-89-20556del
XM_011524629.1:c.-89-20558_-89-20556del XP_011522931.1:n.-89-20558_-89-20556del
XM_011524630.1:c.-89-20558_-89-20556del XP_011522932.1:n.-89-20558_-89-20556del
XM_011524631.1:c.-89-20558_-89-20556del XP_011522933.1:n.-89-20558_-89-20556del
XM_006721823.2:c.-89-20558_-89-20556del XP_006721886.1:n.-89-20558_-89-20556del
XM_006721824.4:c.-89-20558_-89-20556del XP_006721887.1:n.-89-20558_-89-20556del
XM_011524628.3:c.-89-20558_-89-20556del XP_011522930.1:n.-89-20558_-89-20556del
XM_011524629.3:c.-89-20558_-89-20556del XP_011522931.1:n.-89-20558_-89-20556del
XM_011524630.3:c.-89-20558_-89-20556del XP_011522932.1:n.-89-20558_-89-20556del
XM_011524631.3:c.-89-20558_-89-20556del XP_011522933.1:n.-89-20558_-89-20556del
XM_017024488.2:c.-89-20558_-89-20556del XP_016879977.1:n.-89-20558_-89-20556del
XM_017024489.1:c.-90+33_-90+35del XP_016879978.1:n.-90+33_-90+35del
NM_015443.4:c.-90+33_-90+35del MANE Select NP_056258.1:n.-90+33_-90+35del
NM_001193465.2:c.-89-20558_-89-20556del NP_001180394.1:n.-89-20558_-89-20556del
NM_001379198.1:c.-89-20558_-89-20556del NP_001366127.1:n.-89-20558_-89-20556del