Canonical Allele Identifier: CA2262191518

Gene: KANSL1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46192804_46192810delinsGAGCAGC , CM000679.2:g.46192804_46192810delinsGAGCAGC	GRCh38
NC_000017.10:g.44270170_44270176delinsGAGCAGC , CM000679.1:g.44270170_44270176delinsGAGCAGC	GRCh37
NC_000017.9:g.41625947_41625953delinsGAGCAGC	NCBI36
NG_032784.1:g.37565_37571delinsGCTGCTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000432791.7:c.-90+13_-90+19delinsGCTGCTC MANE Select	ENSP00000387393.3:n.-90+13_-90+19delinsGC...
ENST00000571698.2:c.-90+940_-90+946delinsGCTGCTC	ENSP00000459330.2:n.-90+940_-90+946delins...
ENST00000572904.6:c.-89-20578_-89-20572delinsGCTGCTC	ENSP00000461484.1:n.-89-20578_-89-20572de...
ENST00000574590.6:c.-89-20578_-89-20572delinsGCTGCTC	ENSP00000461812.2:n.-89-20578_-89-20572de...
ENST00000574655.6:n.166-20578_166-20572delinsGCTGCTC
ENST00000575318.6:c.-89-20578_-89-20572delinsGCTGCTC	ENSP00000461299.1:n.-89-20578_-89-20572de...
ENST00000576739.2:c.-89-20578_-89-20572delinsGCTGCTC	ENSP00000459627.1:n.-89-20578_-89-20572de...
ENST00000638269.1:n.156-20578_156-20572delinsGCTGCTC
ENST00000638275.1:c.-90+13_-90+19delinsGCTGCTC	ENSP00000492576.1:n.-90+13_-90+19delinsGC...
ENST00000638902.1:n.16-20578_16-20572delinsGCTGCTC
ENST00000639099.1:n.162-20578_162-20572delinsGCTGCTC
ENST00000639150.1:c.23+30861_23+30867delinsGCTGCTC	ENSP00000491906.1:n.23+30861_23+30867deli...
ENST00000639356.1:n.162-20578_162-20572delinsGCTGCTC
ENST00000639375.1:n.150-20578_150-20572delinsGCTGCTC
ENST00000648792.1:c.-89-20578_-89-20572delinsGCTGCTC	ENSP00000497628.1:n.-89-20578_-89-20572de...
ENST00000432791.5:c.-89-20578_-89-20572delinsGCTGCTC	ENSP00000387393.2:n.-89-20578_-89-20572de...
ENST00000571698.1:c.-90+940_-90+946delinsGCTGCTC	ENSP00000459330.1:n.-90+940_-90+946delins...
ENST00000572904.5:c.-90+13_-90+19delinsGCTGCTC	ENSP00000461484.1:n.-90+13_-90+19delinsGC...
ENST00000574590.5:c.-89-20578_-89-20572delinsGCTGCTC	ENSP00000461812.1:n.-89-20578_-89-20572de...
ENST00000574655.5:c.-89-20578_-89-20572delinsGCTGCTC	ENSP00000459359.1:n.-89-20578_-89-20572de...
ENST00000576739.1:c.-89-20578_-89-20572delinsGCTGCTC	ENSP00000459627.1:n.-89-20578_-89-20572de...
NM_001193465.1:c.-89-20578_-89-20572delinsGCTGCTC	NP_001180394.1:n.-89-20578_-89-20572delin...
NM_015443.3:c.-90+13_-90+19delinsGCTGCTC	NP_056258.1:n.-90+13_-90+19delinsGCTGCTC
XM_006721823.1:c.-89-20578_-89-20572delinsGCTGCTC	XP_006721886.1:n.-89-20578_-89-20572delin...
XM_006721824.2:c.-89-20578_-89-20572delinsGCTGCTC	XP_006721887.1:n.-89-20578_-89-20572delin...
XM_011524628.1:c.-89-20578_-89-20572delinsGCTGCTC	XP_011522930.1:n.-89-20578_-89-20572delin...
XM_011524629.1:c.-89-20578_-89-20572delinsGCTGCTC	XP_011522931.1:n.-89-20578_-89-20572delin...
XM_011524630.1:c.-89-20578_-89-20572delinsGCTGCTC	XP_011522932.1:n.-89-20578_-89-20572delin...
XM_011524631.1:c.-89-20578_-89-20572delinsGCTGCTC	XP_011522933.1:n.-89-20578_-89-20572delin...
XM_006721823.2:c.-89-20578_-89-20572delinsGCTGCTC	XP_006721886.1:n.-89-20578_-89-20572delin...
XM_006721824.4:c.-89-20578_-89-20572delinsGCTGCTC	XP_006721887.1:n.-89-20578_-89-20572delin...
XM_011524628.3:c.-89-20578_-89-20572delinsGCTGCTC	XP_011522930.1:n.-89-20578_-89-20572delin...
XM_011524629.3:c.-89-20578_-89-20572delinsGCTGCTC	XP_011522931.1:n.-89-20578_-89-20572delin...
XM_011524630.3:c.-89-20578_-89-20572delinsGCTGCTC	XP_011522932.1:n.-89-20578_-89-20572delin...
XM_011524631.3:c.-89-20578_-89-20572delinsGCTGCTC	XP_011522933.1:n.-89-20578_-89-20572delin...
XM_017024488.2:c.-89-20578_-89-20572delinsGCTGCTC	XP_016879977.1:n.-89-20578_-89-20572delin...
XM_017024489.1:c.-90+13_-90+19delinsGCTGCTC	XP_016879978.1:n.-90+13_-90+19delinsGCTGC...
NM_015443.4:c.-90+13_-90+19delinsGCTGCTC MANE Select	NP_056258.1:n.-90+13_-90+19delinsGCTGCTC
NM_001193465.2:c.-89-20578_-89-20572delinsGCTGCTC	NP_001180394.1:n.-89-20578_-89-20572delin...
NM_001379198.1:c.-89-20578_-89-20572delinsGCTGCTC	NP_001366127.1:n.-89-20578_-89-20572delin...