Canonical Allele Identifier: CA2638372661

Gene: KANSL1

Linked Data

• gnomAD v4: 17-46032320-ATC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46032322_46032323del , CM000679.2:g.46032322_46032323del	GRCh38
NC_000017.10:g.44109688_44109689del , CM000679.1:g.44109688_44109689del	GRCh37
NC_000017.9:g.41465535_41465536del	NCBI36
NG_032784.1:g.198053_198054del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.2838-23_2838-22del MANE Select	ENSP00000387393.3:n.2838-23_2838-22del
ENST00000572904.6:c.2838-23_2838-22del	ENSP00000461484.1:n.2838-23_2838-22del
ENST00000574590.6:c.2835-23_2835-22del	ENSP00000461812.2:n.2835-23_2835-22del
ENST00000575318.6:c.2646-23_2646-22del	ENSP00000461299.1:n.2646-23_2646-22del
ENST00000638275.1:c.2646-23_2646-22del	ENSP00000492576.1:n.2646-23_2646-22del
ENST00000638291.1:n.666-23_666-22del
ENST00000638551.1:n.786-23_786-22del
ENST00000639467.1:c.495-23_495-22del	ENSP00000492741.1:n.495-23_495-22del
ENST00000639531.1:c.2649-23_2649-22del	ENSP00000491765.1:n.2649-23_2649-22del
ENST00000639805.1:n.255-23_255-22del
ENST00000640092.1:n.1525-23_1525-22del
ENST00000640751.1:n.433-23_433-22del
ENST00000648792.1:c.2838-155_2838-154del	ENSP00000497628.1:n.2838-155_2838-154del
ENST00000262419.10:c.2838-23_2838-22del	ENSP00000262419.6:n.2838-23_2838-22del
ENST00000432791.5:c.2835-23_2835-22del	ENSP00000387393.2:n.2835-23_2835-22del
ENST00000572218.5:n.7055-23_7055-22del
ENST00000572904.5:c.2838-23_2838-22del	ENSP00000461484.1:n.2838-23_2838-22del
ENST00000573682.1:n.224-23_224-22del
ENST00000574590.5:c.2838-23_2838-22del	ENSP00000461812.1:n.2838-23_2838-22del
ENST00000574963.1:n.245_246del
ENST00000575318.5:c.2646-23_2646-22del	ENSP00000461299.1:n.2646-23_2646-22del
ENST00000576870.5:n.810-23_810-22del
NM_001193465.1:c.2835-23_2835-22del	NP_001180394.1:n.2835-23_2835-22del
NM_001193466.1:c.2838-23_2838-22del	NP_001180395.1:n.2838-23_2838-22del
NM_015443.3:c.2838-23_2838-22del	NP_056258.1:n.2838-23_2838-22del
XM_006721823.1:c.2838-23_2838-22del	XP_006721886.1:n.2838-23_2838-22del
XM_006721824.2:c.2838-23_2838-22del	XP_006721887.1:n.2838-23_2838-22del
XM_011524628.1:c.2835-23_2835-22del	XP_011522930.1:n.2835-23_2835-22del
XM_011524629.1:c.2736-23_2736-22del	XP_011522931.1:n.2736-23_2736-22del
XM_011524630.1:c.2649-23_2649-22del	XP_011522932.1:n.2649-23_2649-22del
XM_011524631.1:c.2646-23_2646-22del	XP_011522933.1:n.2646-23_2646-22del
XM_011524632.1:c.1608-23_1608-22del	XP_011522934.1:n.1608-23_1608-22del
XM_006721823.2:c.2838-23_2838-22del	XP_006721886.1:n.2838-23_2838-22del
XM_006721824.4:c.2838-23_2838-22del	XP_006721887.1:n.2838-23_2838-22del
XM_011524628.3:c.2835-23_2835-22del	XP_011522930.1:n.2835-23_2835-22del
XM_011524629.3:c.2736-23_2736-22del	XP_011522931.1:n.2736-23_2736-22del
XM_011524630.3:c.2649-23_2649-22del	XP_011522932.1:n.2649-23_2649-22del
XM_011524631.3:c.2646-23_2646-22del	XP_011522933.1:n.2646-23_2646-22del
XM_011524632.3:c.1608-23_1608-22del	XP_011522934.1:n.1608-23_1608-22del
XM_017024488.2:c.2646-23_2646-22del	XP_016879977.1:n.2646-23_2646-22del
NM_001193466.2:c.2838-23_2838-22del	NP_001180395.1:n.2838-23_2838-22del
NM_015443.4:c.2838-23_2838-22del MANE Select	NP_056258.1:n.2838-23_2838-22del
NM_001193465.2:c.2835-23_2835-22del	NP_001180394.1:n.2835-23_2835-22del
NM_001379198.1:c.2838-23_2838-22del	NP_001366127.1:n.2838-23_2838-22del