Canonical Allele Identifier: CA2262191374

Gene: KANSL1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46192604_46192605delinsAG , CM000679.2:g.46192604_46192605delinsAG	GRCh38
NC_000017.10:g.44269970_44269971delinsAG , CM000679.1:g.44269970_44269971delinsAG	GRCh37
NC_000017.9:g.41625747_41625748delinsAG	NCBI36
NG_032784.1:g.37770_37771delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.-90+218_-90+219delinsCT MANE Select	ENSP00000387393.3:n.-90+218_-90+219delinsCT
ENST00000571698.2:c.-90+1145_-90+1146delinsCT	ENSP00000459330.2:n.-90+1145_-90+1146delinsCT
ENST00000572904.6:c.-89-20373_-89-20372delinsCT	ENSP00000461484.1:n.-89-20373_-89-20372delinsCT
ENST00000574590.6:c.-89-20373_-89-20372delinsCT	ENSP00000461812.2:n.-89-20373_-89-20372delinsCT
ENST00000574655.6:n.166-20373_166-20372delinsCT
ENST00000575318.6:c.-89-20373_-89-20372delinsCT	ENSP00000461299.1:n.-89-20373_-89-20372delinsCT
ENST00000576739.2:c.-89-20373_-89-20372delinsCT	ENSP00000459627.1:n.-89-20373_-89-20372delinsCT
ENST00000638269.1:n.156-20373_156-20372delinsCT
ENST00000638275.1:c.-90+218_-90+219delinsCT	ENSP00000492576.1:n.-90+218_-90+219delinsCT
ENST00000638902.1:n.16-20373_16-20372delinsCT
ENST00000639099.1:n.162-20373_162-20372delinsCT
ENST00000639150.1:c.23+31066_23+31067delinsCT	ENSP00000491906.1:n.23+31066_23+31067delinsCT
ENST00000639356.1:n.162-20373_162-20372delinsCT
ENST00000639375.1:n.150-20373_150-20372delinsCT
ENST00000648792.1:c.-89-20373_-89-20372delinsCT	ENSP00000497628.1:n.-89-20373_-89-20372delinsCT
ENST00000262419.10:c.-276_-275delinsCT	ENSP00000262419.6:n.-276_-275delinsCT
ENST00000432791.5:c.-89-20373_-89-20372delinsCT	ENSP00000387393.2:n.-89-20373_-89-20372delinsCT
ENST00000571698.1:c.-90+1145_-90+1146delinsCT	ENSP00000459330.1:n.-90+1145_-90+1146delinsCT
ENST00000572904.5:c.-90+218_-90+219delinsCT	ENSP00000461484.1:n.-90+218_-90+219delinsCT
ENST00000574590.5:c.-89-20373_-89-20372delinsCT	ENSP00000461812.1:n.-89-20373_-89-20372delinsCT
ENST00000574655.5:c.-89-20373_-89-20372delinsCT	ENSP00000459359.1:n.-89-20373_-89-20372delinsCT
ENST00000576739.1:c.-89-20373_-89-20372delinsCT	ENSP00000459627.1:n.-89-20373_-89-20372delinsCT
NM_001193465.1:c.-89-20373_-89-20372delinsCT	NP_001180394.1:n.-89-20373_-89-20372delinsCT
NM_001193466.1:c.-276_-275delinsCT	NP_001180395.1:n.-276_-275delinsCT
NM_015443.3:c.-90+218_-90+219delinsCT	NP_056258.1:n.-90+218_-90+219delinsCT
XM_006721823.1:c.-89-20373_-89-20372delinsCT	XP_006721886.1:n.-89-20373_-89-20372delinsCT
XM_006721824.2:c.-89-20373_-89-20372delinsCT	XP_006721887.1:n.-89-20373_-89-20372delinsCT
XM_011524628.1:c.-89-20373_-89-20372delinsCT	XP_011522930.1:n.-89-20373_-89-20372delinsCT
XM_011524629.1:c.-89-20373_-89-20372delinsCT	XP_011522931.1:n.-89-20373_-89-20372delinsCT
XM_011524630.1:c.-89-20373_-89-20372delinsCT	XP_011522932.1:n.-89-20373_-89-20372delinsCT
XM_011524631.1:c.-89-20373_-89-20372delinsCT	XP_011522933.1:n.-89-20373_-89-20372delinsCT
XM_006721823.2:c.-89-20373_-89-20372delinsCT	XP_006721886.1:n.-89-20373_-89-20372delinsCT
XM_006721824.4:c.-89-20373_-89-20372delinsCT	XP_006721887.1:n.-89-20373_-89-20372delinsCT
XM_011524628.3:c.-89-20373_-89-20372delinsCT	XP_011522930.1:n.-89-20373_-89-20372delinsCT
XM_011524629.3:c.-89-20373_-89-20372delinsCT	XP_011522931.1:n.-89-20373_-89-20372delinsCT
XM_011524630.3:c.-89-20373_-89-20372delinsCT	XP_011522932.1:n.-89-20373_-89-20372delinsCT
XM_011524631.3:c.-89-20373_-89-20372delinsCT	XP_011522933.1:n.-89-20373_-89-20372delinsCT
XM_017024488.2:c.-89-20373_-89-20372delinsCT	XP_016879977.1:n.-89-20373_-89-20372delinsCT
XM_017024489.1:c.-90+218_-90+219delinsCT	XP_016879978.1:n.-90+218_-90+219delinsCT
NM_001193466.2:c.-276_-275delinsCT	NP_001180395.1:n.-276_-275delinsCT
NM_015443.4:c.-90+218_-90+219delinsCT MANE Select	NP_056258.1:n.-90+218_-90+219delinsCT
NM_001193465.2:c.-89-20373_-89-20372delinsCT	NP_001180394.1:n.-89-20373_-89-20372delinsCT
NM_001379198.1:c.-89-20373_-89-20372delinsCT	NP_001366127.1:n.-89-20373_-89-20372delinsCT