Canonical Allele Identifier: CA2809645155

Gene: KANSL1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46193152_46193153insAGGG , CM000679.2:g.46193152_46193153insAGGG	GRCh38
NC_000017.10:g.44270518_44270519insAGGG , CM000679.1:g.44270518_44270519insAGGG	GRCh37
NC_000017.9:g.41626295_41626296insAGGG	NCBI36
NG_032784.1:g.37225_37226insTCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.-417_-416insTCCC MANE Select	ENSP00000387393.3:n.-417_-416insTCCC
ENST00000571698.2:c.-90+600_-90+601insTCCC	ENSP00000459330.2:n.-90+600_-90+601insTCCC
ENST00000572904.6:c.-89-20918_-89-20917insTCCC	ENSP00000461484.1:n.-89-20918_-89-20917insTCCC
ENST00000574590.6:c.-89-20918_-89-20917insTCCC	ENSP00000461812.2:n.-89-20918_-89-20917insTCCC
ENST00000574655.6:n.166-20918_166-20917insTCCC
ENST00000575318.6:c.-89-20918_-89-20917insTCCC	ENSP00000461299.1:n.-89-20918_-89-20917insTCCC
ENST00000576739.2:c.-89-20918_-89-20917insTCCC	ENSP00000459627.1:n.-89-20918_-89-20917insTCCC
ENST00000638269.1:n.156-20918_156-20917insTCCC
ENST00000638275.1:c.-417_-416insTCCC	ENSP00000492576.1:n.-417_-416insTCCC
ENST00000638902.1:n.16-20918_16-20917insTCCC
ENST00000639099.1:n.162-20918_162-20917insTCCC
ENST00000639150.1:c.23+30521_23+30522insTCCC	ENSP00000491906.1:n.23+30521_23+30522insTCCC
ENST00000639356.1:n.162-20918_162-20917insTCCC
ENST00000639375.1:n.150-20918_150-20917insTCCC
ENST00000648792.1:c.-89-20918_-89-20917insTCCC	ENSP00000497628.1:n.-89-20918_-89-20917insTCCC
ENST00000432791.5:c.-89-20918_-89-20917insTCCC	ENSP00000387393.2:n.-89-20918_-89-20917insTCCC
ENST00000571698.1:c.-90+600_-90+601insTCCC	ENSP00000459330.1:n.-90+600_-90+601insTCCC
ENST00000574590.5:c.-89-20918_-89-20917insTCCC	ENSP00000461812.1:n.-89-20918_-89-20917insTCCC
ENST00000574655.5:c.-89-20918_-89-20917insTCCC	ENSP00000459359.1:n.-89-20918_-89-20917insTCCC
ENST00000576739.1:c.-89-20918_-89-20917insTCCC	ENSP00000459627.1:n.-89-20918_-89-20917insTCCC
NM_001193465.1:c.-89-20918_-89-20917insTCCC	NP_001180394.1:n.-89-20918_-89-20917insTCCC
XM_006721823.1:c.-89-20918_-89-20917insTCCC	XP_006721886.1:n.-89-20918_-89-20917insTCCC
XM_006721824.2:c.-89-20918_-89-20917insTCCC	XP_006721887.1:n.-89-20918_-89-20917insTCCC
XM_011524628.1:c.-89-20918_-89-20917insTCCC	XP_011522930.1:n.-89-20918_-89-20917insTCCC
XM_011524629.1:c.-89-20918_-89-20917insTCCC	XP_011522931.1:n.-89-20918_-89-20917insTCCC
XM_011524630.1:c.-89-20918_-89-20917insTCCC	XP_011522932.1:n.-89-20918_-89-20917insTCCC
XM_011524631.1:c.-89-20918_-89-20917insTCCC	XP_011522933.1:n.-89-20918_-89-20917insTCCC
XM_006721823.2:c.-89-20918_-89-20917insTCCC	XP_006721886.1:n.-89-20918_-89-20917insTCCC
XM_006721824.4:c.-89-20918_-89-20917insTCCC	XP_006721887.1:n.-89-20918_-89-20917insTCCC
XM_011524628.3:c.-89-20918_-89-20917insTCCC	XP_011522930.1:n.-89-20918_-89-20917insTCCC
XM_011524629.3:c.-89-20918_-89-20917insTCCC	XP_011522931.1:n.-89-20918_-89-20917insTCCC
XM_011524630.3:c.-89-20918_-89-20917insTCCC	XP_011522932.1:n.-89-20918_-89-20917insTCCC
XM_011524631.3:c.-89-20918_-89-20917insTCCC	XP_011522933.1:n.-89-20918_-89-20917insTCCC
XM_017024488.2:c.-89-20918_-89-20917insTCCC	XP_016879977.1:n.-89-20918_-89-20917insTCCC
NM_015443.4:c.-417_-416insTCCC MANE Select	NP_056258.1:n.-417_-416insTCCC
NM_001193465.2:c.-89-20918_-89-20917insTCCC	NP_001180394.1:n.-89-20918_-89-20917insTCCC
NM_001379198.1:c.-89-20918_-89-20917insTCCC	NP_001366127.1:n.-89-20918_-89-20917insTCCC