Canonical Allele Identifier: CA2262191895

Gene: KANSL1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46193219_46193220delinsAC , CM000679.2:g.46193219_46193220delinsAC	GRCh38
NC_000017.10:g.44270585_44270586delinsAC , CM000679.1:g.44270585_44270586delinsAC	GRCh37
NC_000017.9:g.41626362_41626363delinsAC	NCBI36
NG_032784.1:g.37155_37156delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.-487_-486delinsGT MANE Select	ENSP00000387393.3:n.-487_-486delinsGT
ENST00000571698.2:c.-90+530_-90+531delinsGT	ENSP00000459330.2:n.-90+530_-90+531delinsGT
ENST00000572904.6:c.-89-20988_-89-20987delinsGT	ENSP00000461484.1:n.-89-20988_-89-20987delinsGT
ENST00000574590.6:c.-89-20988_-89-20987delinsGT	ENSP00000461812.2:n.-89-20988_-89-20987delinsGT
ENST00000574655.6:n.166-20988_166-20987delinsGT
ENST00000575318.6:c.-89-20988_-89-20987delinsGT	ENSP00000461299.1:n.-89-20988_-89-20987delinsGT
ENST00000576739.2:c.-89-20988_-89-20987delinsGT	ENSP00000459627.1:n.-89-20988_-89-20987delinsGT
ENST00000638269.1:n.156-20988_156-20987delinsGT
ENST00000638275.1:c.-487_-486delinsGT	ENSP00000492576.1:n.-487_-486delinsGT
ENST00000638902.1:n.16-20988_16-20987delinsGT
ENST00000639099.1:n.162-20988_162-20987delinsGT
ENST00000639150.1:c.23+30451_23+30452delinsGT	ENSP00000491906.1:n.23+30451_23+30452delinsGT
ENST00000639356.1:n.162-20988_162-20987delinsGT
ENST00000639375.1:n.150-20988_150-20987delinsGT
ENST00000648792.1:c.-89-20988_-89-20987delinsGT	ENSP00000497628.1:n.-89-20988_-89-20987delinsGT
ENST00000432791.5:c.-89-20988_-89-20987delinsGT	ENSP00000387393.2:n.-89-20988_-89-20987delinsGT
ENST00000571698.1:c.-90+530_-90+531delinsGT	ENSP00000459330.1:n.-90+530_-90+531delinsGT
ENST00000574590.5:c.-89-20988_-89-20987delinsGT	ENSP00000461812.1:n.-89-20988_-89-20987delinsGT
ENST00000574655.5:c.-89-20988_-89-20987delinsGT	ENSP00000459359.1:n.-89-20988_-89-20987delinsGT
ENST00000576739.1:c.-89-20988_-89-20987delinsGT	ENSP00000459627.1:n.-89-20988_-89-20987delinsGT
NM_001193465.1:c.-89-20988_-89-20987delinsGT	NP_001180394.1:n.-89-20988_-89-20987delinsGT
XM_006721823.1:c.-89-20988_-89-20987delinsGT	XP_006721886.1:n.-89-20988_-89-20987delinsGT
XM_006721824.2:c.-89-20988_-89-20987delinsGT	XP_006721887.1:n.-89-20988_-89-20987delinsGT
XM_011524628.1:c.-89-20988_-89-20987delinsGT	XP_011522930.1:n.-89-20988_-89-20987delinsGT
XM_011524629.1:c.-89-20988_-89-20987delinsGT	XP_011522931.1:n.-89-20988_-89-20987delinsGT
XM_011524630.1:c.-89-20988_-89-20987delinsGT	XP_011522932.1:n.-89-20988_-89-20987delinsGT
XM_011524631.1:c.-89-20988_-89-20987delinsGT	XP_011522933.1:n.-89-20988_-89-20987delinsGT
XM_006721823.2:c.-89-20988_-89-20987delinsGT	XP_006721886.1:n.-89-20988_-89-20987delinsGT
XM_006721824.4:c.-89-20988_-89-20987delinsGT	XP_006721887.1:n.-89-20988_-89-20987delinsGT
XM_011524628.3:c.-89-20988_-89-20987delinsGT	XP_011522930.1:n.-89-20988_-89-20987delinsGT
XM_011524629.3:c.-89-20988_-89-20987delinsGT	XP_011522931.1:n.-89-20988_-89-20987delinsGT
XM_011524630.3:c.-89-20988_-89-20987delinsGT	XP_011522932.1:n.-89-20988_-89-20987delinsGT
XM_011524631.3:c.-89-20988_-89-20987delinsGT	XP_011522933.1:n.-89-20988_-89-20987delinsGT
XM_017024488.2:c.-89-20988_-89-20987delinsGT	XP_016879977.1:n.-89-20988_-89-20987delinsGT
NM_015443.4:c.-487_-486delinsGT MANE Select	NP_056258.1:n.-487_-486delinsGT
NM_001193465.2:c.-89-20988_-89-20987delinsGT	NP_001180394.1:n.-89-20988_-89-20987delinsGT
NM_001379198.1:c.-89-20988_-89-20987delinsGT	NP_001366127.1:n.-89-20988_-89-20987delinsGT