Canonical Allele Identifier: CA2638373444

Gene: KANSL1

Linked Data

• gnomAD v4: 17-46032590-CAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46032592_46032593del , CM000679.2:g.46032592_46032593del	GRCh38
NC_000017.10:g.44109958_44109959del , CM000679.1:g.44109958_44109959del	GRCh37
NC_000017.9:g.41465805_41465806del	NCBI36
NG_032784.1:g.197783_197784del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.2838-293_2838-292del MANE Select	ENSP00000387393.3:n.2838-293_2838-292del
ENST00000572904.6:c.2838-293_2838-292del	ENSP00000461484.1:n.2838-293_2838-292del
ENST00000574590.6:c.2835-293_2835-292del	ENSP00000461812.2:n.2835-293_2835-292del
ENST00000575318.6:c.2646-293_2646-292del	ENSP00000461299.1:n.2646-293_2646-292del
ENST00000638275.1:c.2646-293_2646-292del	ENSP00000492576.1:n.2646-293_2646-292del
ENST00000638291.1:n.666-293_666-292del
ENST00000638551.1:n.786-293_786-292del
ENST00000639467.1:c.495-293_495-292del	ENSP00000492741.1:n.495-293_495-292del
ENST00000639531.1:c.2649-293_2649-292del	ENSP00000491765.1:n.2649-293_2649-292del
ENST00000639805.1:n.255-293_255-292del
ENST00000640092.1:n.1525-293_1525-292del
ENST00000640751.1:n.433-293_433-292del
ENST00000648792.1:c.2838-425_2838-424del	ENSP00000497628.1:n.2838-425_2838-424del
ENST00000262419.10:c.2838-293_2838-292del	ENSP00000262419.6:n.2838-293_2838-292del
ENST00000432791.5:c.2835-293_2835-292del	ENSP00000387393.2:n.2835-293_2835-292del
ENST00000572218.5:n.7055-293_7055-292del
ENST00000572904.5:c.2838-293_2838-292del	ENSP00000461484.1:n.2838-293_2838-292del
ENST00000573682.1:n.224-293_224-292del
ENST00000574590.5:c.2838-293_2838-292del	ENSP00000461812.1:n.2838-293_2838-292del
ENST00000575318.5:c.2646-293_2646-292del	ENSP00000461299.1:n.2646-293_2646-292del
ENST00000576870.5:n.810-293_810-292del
NM_001193465.1:c.2835-293_2835-292del	NP_001180394.1:n.2835-293_2835-292del
NM_001193466.1:c.2838-293_2838-292del	NP_001180395.1:n.2838-293_2838-292del
NM_015443.3:c.2838-293_2838-292del	NP_056258.1:n.2838-293_2838-292del
XM_006721823.1:c.2838-293_2838-292del	XP_006721886.1:n.2838-293_2838-292del
XM_006721824.2:c.2838-293_2838-292del	XP_006721887.1:n.2838-293_2838-292del
XM_011524628.1:c.2835-293_2835-292del	XP_011522930.1:n.2835-293_2835-292del
XM_011524629.1:c.2736-293_2736-292del	XP_011522931.1:n.2736-293_2736-292del
XM_011524630.1:c.2649-293_2649-292del	XP_011522932.1:n.2649-293_2649-292del
XM_011524631.1:c.2646-293_2646-292del	XP_011522933.1:n.2646-293_2646-292del
XM_011524632.1:c.1608-293_1608-292del	XP_011522934.1:n.1608-293_1608-292del
XM_006721823.2:c.2838-293_2838-292del	XP_006721886.1:n.2838-293_2838-292del
XM_006721824.4:c.2838-293_2838-292del	XP_006721887.1:n.2838-293_2838-292del
XM_011524628.3:c.2835-293_2835-292del	XP_011522930.1:n.2835-293_2835-292del
XM_011524629.3:c.2736-293_2736-292del	XP_011522931.1:n.2736-293_2736-292del
XM_011524630.3:c.2649-293_2649-292del	XP_011522932.1:n.2649-293_2649-292del
XM_011524631.3:c.2646-293_2646-292del	XP_011522933.1:n.2646-293_2646-292del
XM_011524632.3:c.1608-293_1608-292del	XP_011522934.1:n.1608-293_1608-292del
XM_017024488.2:c.2646-293_2646-292del	XP_016879977.1:n.2646-293_2646-292del
NM_001193466.2:c.2838-293_2838-292del	NP_001180395.1:n.2838-293_2838-292del
NM_015443.4:c.2838-293_2838-292del MANE Select	NP_056258.1:n.2838-293_2838-292del
NM_001193465.2:c.2835-293_2835-292del	NP_001180394.1:n.2835-293_2835-292del
NM_001379198.1:c.2838-293_2838-292del	NP_001366127.1:n.2838-293_2838-292del