Canonical Allele Identifier: CA2262111193

Gene: KANSL1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46032548_46032551delinsCAGG , CM000679.2:g.46032548_46032551delinsCAGG	GRCh38
NC_000017.10:g.44109914_44109917delinsCAGG , CM000679.1:g.44109914_44109917delinsCAGG	GRCh37
NC_000017.9:g.41465761_41465764delinsCAGG	NCBI36
NG_032784.1:g.197824_197827delinsCCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.2838-252_2838-249delinsCCTG MANE Select	ENSP00000387393.3:n.2838-252_2838-249delinsCCTG
ENST00000572904.6:c.2838-252_2838-249delinsCCTG	ENSP00000461484.1:n.2838-252_2838-249delinsCCTG
ENST00000574590.6:c.2835-252_2835-249delinsCCTG	ENSP00000461812.2:n.2835-252_2835-249delinsCCTG
ENST00000575318.6:c.2646-252_2646-249delinsCCTG	ENSP00000461299.1:n.2646-252_2646-249delinsCCTG
ENST00000638275.1:c.2646-252_2646-249delinsCCTG	ENSP00000492576.1:n.2646-252_2646-249delinsCCTG
ENST00000638291.1:n.666-252_666-249delinsCCTG
ENST00000638551.1:n.786-252_786-249delinsCCTG
ENST00000639467.1:c.495-252_495-249delinsCCTG	ENSP00000492741.1:n.495-252_495-249delinsCCTG
ENST00000639531.1:c.2649-252_2649-249delinsCCTG	ENSP00000491765.1:n.2649-252_2649-249delinsCCTG
ENST00000639805.1:n.255-252_255-249delinsCCTG
ENST00000640092.1:n.1525-252_1525-249delinsCCTG
ENST00000640751.1:n.433-252_433-249delinsCCTG
ENST00000648792.1:c.2838-384_2838-381delinsCCTG	ENSP00000497628.1:n.2838-384_2838-381delinsCCTG
ENST00000262419.10:c.2838-252_2838-249delinsCCTG	ENSP00000262419.6:n.2838-252_2838-249delinsCCTG
ENST00000432791.5:c.2835-252_2835-249delinsCCTG	ENSP00000387393.2:n.2835-252_2835-249delinsCCTG
ENST00000572218.5:n.7055-252_7055-249delinsCCTG
ENST00000572904.5:c.2838-252_2838-249delinsCCTG	ENSP00000461484.1:n.2838-252_2838-249delinsCCTG
ENST00000573682.1:n.224-252_224-249delinsCCTG
ENST00000574590.5:c.2838-252_2838-249delinsCCTG	ENSP00000461812.1:n.2838-252_2838-249delinsCCTG
ENST00000574963.1:n.16_19delinsCCTG
ENST00000575318.5:c.2646-252_2646-249delinsCCTG	ENSP00000461299.1:n.2646-252_2646-249delinsCCTG
ENST00000576870.5:n.810-252_810-249delinsCCTG
NM_001193465.1:c.2835-252_2835-249delinsCCTG	NP_001180394.1:n.2835-252_2835-249delinsCCTG
NM_001193466.1:c.2838-252_2838-249delinsCCTG	NP_001180395.1:n.2838-252_2838-249delinsCCTG
NM_015443.3:c.2838-252_2838-249delinsCCTG	NP_056258.1:n.2838-252_2838-249delinsCCTG
XM_006721823.1:c.2838-252_2838-249delinsCCTG	XP_006721886.1:n.2838-252_2838-249delinsCCTG
XM_006721824.2:c.2838-252_2838-249delinsCCTG	XP_006721887.1:n.2838-252_2838-249delinsCCTG
XM_011524628.1:c.2835-252_2835-249delinsCCTG	XP_011522930.1:n.2835-252_2835-249delinsCCTG
XM_011524629.1:c.2736-252_2736-249delinsCCTG	XP_011522931.1:n.2736-252_2736-249delinsCCTG
XM_011524630.1:c.2649-252_2649-249delinsCCTG	XP_011522932.1:n.2649-252_2649-249delinsCCTG
XM_011524631.1:c.2646-252_2646-249delinsCCTG	XP_011522933.1:n.2646-252_2646-249delinsCCTG
XM_011524632.1:c.1608-252_1608-249delinsCCTG	XP_011522934.1:n.1608-252_1608-249delinsCCTG
XM_006721823.2:c.2838-252_2838-249delinsCCTG	XP_006721886.1:n.2838-252_2838-249delinsCCTG
XM_006721824.4:c.2838-252_2838-249delinsCCTG	XP_006721887.1:n.2838-252_2838-249delinsCCTG
XM_011524628.3:c.2835-252_2835-249delinsCCTG	XP_011522930.1:n.2835-252_2835-249delinsCCTG
XM_011524629.3:c.2736-252_2736-249delinsCCTG	XP_011522931.1:n.2736-252_2736-249delinsCCTG
XM_011524630.3:c.2649-252_2649-249delinsCCTG	XP_011522932.1:n.2649-252_2649-249delinsCCTG
XM_011524631.3:c.2646-252_2646-249delinsCCTG	XP_011522933.1:n.2646-252_2646-249delinsCCTG
XM_011524632.3:c.1608-252_1608-249delinsCCTG	XP_011522934.1:n.1608-252_1608-249delinsCCTG
XM_017024488.2:c.2646-252_2646-249delinsCCTG	XP_016879977.1:n.2646-252_2646-249delinsCCTG
NM_001193466.2:c.2838-252_2838-249delinsCCTG	NP_001180395.1:n.2838-252_2838-249delinsCCTG
NM_015443.4:c.2838-252_2838-249delinsCCTG MANE Select	NP_056258.1:n.2838-252_2838-249delinsCCTG
NM_001193465.2:c.2835-252_2835-249delinsCCTG	NP_001180394.1:n.2835-252_2835-249delinsCCTG
NM_001379198.1:c.2838-252_2838-249delinsCCTG	NP_001366127.1:n.2838-252_2838-249delinsCCTG