Canonical Allele Identifier: CA2262191829
Gene: KANSL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46193137_46193153delinsAGGGCGGGCGGGCGGGG , CM000679.2:g.46193137_46193153delinsAGGGCGGGCGGGCGGGG GRCh38
NC_000017.10:g.44270503_44270519delinsAGGGCGGGCGGGCGGGG , CM000679.1:g.44270503_44270519delinsAGGGCGGGCGGGCGGGG GRCh37
NC_000017.9:g.41626280_41626296delinsAGGGCGGGCGGGCGGGG NCBI36
NG_032784.1:g.37222_37238delinsCCCCGCCCGCCCGCCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000432791.7:c.-420_-404delinsCCCCGCCCGCCCGCCCT MANE Select ENSP00000387393.3:n.-420_-404delinsCCCCGCCCGCCCGCCCT
ENST00000571698.2:c.-90+597_-90+613delinsCCCCGCCCGCCCGCCCT ENSP00000459330.2:n.-90+597_-90+613delinsCCCCGCCCGCCCGCCCT
ENST00000572904.6:c.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT ENSP00000461484.1:n.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCC...
ENST00000574590.6:c.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT ENSP00000461812.2:n.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCC...
ENST00000574655.6:n.166-20921_166-20905delinsCCCCGCCCGCCCGCCCT
ENST00000575318.6:c.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT ENSP00000461299.1:n.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCC...
ENST00000576739.2:c.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT ENSP00000459627.1:n.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCC...
ENST00000638269.1:n.156-20921_156-20905delinsCCCCGCCCGCCCGCCCT
ENST00000638275.1:c.-420_-404delinsCCCCGCCCGCCCGCCCT ENSP00000492576.1:n.-420_-404delinsCCCCGCCCGCCCGCCCT
ENST00000638902.1:n.16-20921_16-20905delinsCCCCGCCCGCCCGCCCT
ENST00000639099.1:n.162-20921_162-20905delinsCCCCGCCCGCCCGCCCT
ENST00000639150.1:c.23+30518_23+30534delinsCCCCGCCCGCCCGCCCT ENSP00000491906.1:n.23+30518_23+30534delinsCCCCGCCCGCCCGCCCT
ENST00000639356.1:n.162-20921_162-20905delinsCCCCGCCCGCCCGCCCT
ENST00000639375.1:n.150-20921_150-20905delinsCCCCGCCCGCCCGCCCT
ENST00000648792.1:c.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT ENSP00000497628.1:n.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCC...
ENST00000432791.5:c.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT ENSP00000387393.2:n.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCC...
ENST00000571698.1:c.-90+597_-90+613delinsCCCCGCCCGCCCGCCCT ENSP00000459330.1:n.-90+597_-90+613delinsCCCCGCCCGCCCGCCCT
ENST00000574590.5:c.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT ENSP00000461812.1:n.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCC...
ENST00000574655.5:c.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT ENSP00000459359.1:n.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCC...
ENST00000576739.1:c.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT ENSP00000459627.1:n.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCC...
NM_001193465.1:c.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT NP_001180394.1:n.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT
XM_006721823.1:c.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT XP_006721886.1:n.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT
XM_006721824.2:c.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT XP_006721887.1:n.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT
XM_011524628.1:c.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT XP_011522930.1:n.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT
XM_011524629.1:c.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT XP_011522931.1:n.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT
XM_011524630.1:c.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT XP_011522932.1:n.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT
XM_011524631.1:c.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT XP_011522933.1:n.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT
XM_006721823.2:c.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT XP_006721886.1:n.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT
XM_006721824.4:c.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT XP_006721887.1:n.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT
XM_011524628.3:c.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT XP_011522930.1:n.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT
XM_011524629.3:c.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT XP_011522931.1:n.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT
XM_011524630.3:c.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT XP_011522932.1:n.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT
XM_011524631.3:c.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT XP_011522933.1:n.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT
XM_017024488.2:c.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT XP_016879977.1:n.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT
NM_015443.4:c.-420_-404delinsCCCCGCCCGCCCGCCCT MANE Select NP_056258.1:n.-420_-404delinsCCCCGCCCGCCCGCCCT
NM_001193465.2:c.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT NP_001180394.1:n.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT
NM_001379198.1:c.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT NP_001366127.1:n.-89-20921_-89-20905delinsCCCCGCCCGCCCGCCCT