Canonical Allele Identifier: CA2262111165

Gene: KANSL1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46032466_46032467delinsAG , CM000679.2:g.46032466_46032467delinsAG	GRCh38
NC_000017.10:g.44109832_44109833delinsAG , CM000679.1:g.44109832_44109833delinsAG	GRCh37
NC_000017.9:g.41465679_41465680delinsAG	NCBI36
NG_032784.1:g.197908_197909delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.2838-168_2838-167delinsCT MANE Select	ENSP00000387393.3:n.2838-168_2838-167delinsCT
ENST00000572904.6:c.2838-168_2838-167delinsCT	ENSP00000461484.1:n.2838-168_2838-167delinsCT
ENST00000574590.6:c.2835-168_2835-167delinsCT	ENSP00000461812.2:n.2835-168_2835-167delinsCT
ENST00000575318.6:c.2646-168_2646-167delinsCT	ENSP00000461299.1:n.2646-168_2646-167delinsCT
ENST00000638275.1:c.2646-168_2646-167delinsCT	ENSP00000492576.1:n.2646-168_2646-167delinsCT
ENST00000638291.1:n.666-168_666-167delinsCT
ENST00000638551.1:n.786-168_786-167delinsCT
ENST00000639467.1:c.495-168_495-167delinsCT	ENSP00000492741.1:n.495-168_495-167delinsCT
ENST00000639531.1:c.2649-168_2649-167delinsCT	ENSP00000491765.1:n.2649-168_2649-167delinsCT
ENST00000639805.1:n.255-168_255-167delinsCT
ENST00000640092.1:n.1525-168_1525-167delinsCT
ENST00000640751.1:n.433-168_433-167delinsCT
ENST00000648792.1:c.2838-300_2838-299delinsCT	ENSP00000497628.1:n.2838-300_2838-299delinsCT
ENST00000262419.10:c.2838-168_2838-167delinsCT	ENSP00000262419.6:n.2838-168_2838-167delinsCT
ENST00000432791.5:c.2835-168_2835-167delinsCT	ENSP00000387393.2:n.2835-168_2835-167delinsCT
ENST00000572218.5:n.7055-168_7055-167delinsCT
ENST00000572904.5:c.2838-168_2838-167delinsCT	ENSP00000461484.1:n.2838-168_2838-167delinsCT
ENST00000573682.1:n.224-168_224-167delinsCT
ENST00000574590.5:c.2838-168_2838-167delinsCT	ENSP00000461812.1:n.2838-168_2838-167delinsCT
ENST00000574963.1:n.100_101delinsCT
ENST00000575318.5:c.2646-168_2646-167delinsCT	ENSP00000461299.1:n.2646-168_2646-167delinsCT
ENST00000576870.5:n.810-168_810-167delinsCT
NM_001193465.1:c.2835-168_2835-167delinsCT	NP_001180394.1:n.2835-168_2835-167delinsCT
NM_001193466.1:c.2838-168_2838-167delinsCT	NP_001180395.1:n.2838-168_2838-167delinsCT
NM_015443.3:c.2838-168_2838-167delinsCT	NP_056258.1:n.2838-168_2838-167delinsCT
XM_006721823.1:c.2838-168_2838-167delinsCT	XP_006721886.1:n.2838-168_2838-167delinsCT
XM_006721824.2:c.2838-168_2838-167delinsCT	XP_006721887.1:n.2838-168_2838-167delinsCT
XM_011524628.1:c.2835-168_2835-167delinsCT	XP_011522930.1:n.2835-168_2835-167delinsCT
XM_011524629.1:c.2736-168_2736-167delinsCT	XP_011522931.1:n.2736-168_2736-167delinsCT
XM_011524630.1:c.2649-168_2649-167delinsCT	XP_011522932.1:n.2649-168_2649-167delinsCT
XM_011524631.1:c.2646-168_2646-167delinsCT	XP_011522933.1:n.2646-168_2646-167delinsCT
XM_011524632.1:c.1608-168_1608-167delinsCT	XP_011522934.1:n.1608-168_1608-167delinsCT
XM_006721823.2:c.2838-168_2838-167delinsCT	XP_006721886.1:n.2838-168_2838-167delinsCT
XM_006721824.4:c.2838-168_2838-167delinsCT	XP_006721887.1:n.2838-168_2838-167delinsCT
XM_011524628.3:c.2835-168_2835-167delinsCT	XP_011522930.1:n.2835-168_2835-167delinsCT
XM_011524629.3:c.2736-168_2736-167delinsCT	XP_011522931.1:n.2736-168_2736-167delinsCT
XM_011524630.3:c.2649-168_2649-167delinsCT	XP_011522932.1:n.2649-168_2649-167delinsCT
XM_011524631.3:c.2646-168_2646-167delinsCT	XP_011522933.1:n.2646-168_2646-167delinsCT
XM_011524632.3:c.1608-168_1608-167delinsCT	XP_011522934.1:n.1608-168_1608-167delinsCT
XM_017024488.2:c.2646-168_2646-167delinsCT	XP_016879977.1:n.2646-168_2646-167delinsCT
NM_001193466.2:c.2838-168_2838-167delinsCT	NP_001180395.1:n.2838-168_2838-167delinsCT
NM_015443.4:c.2838-168_2838-167delinsCT MANE Select	NP_056258.1:n.2838-168_2838-167delinsCT
NM_001193465.2:c.2835-168_2835-167delinsCT	NP_001180394.1:n.2835-168_2835-167delinsCT
NM_001379198.1:c.2838-168_2838-167delinsCT	NP_001366127.1:n.2838-168_2838-167delinsCT