Canonical Allele Identifier: CA2638373458

Gene: KANSL1

Linked Data

• gnomAD v4: 17-46032595-A-ATCATT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46032595_46032596insTCATT , CM000679.2:g.46032595_46032596insTCATT	GRCh38
NC_000017.10:g.44109961_44109962insTCATT , CM000679.1:g.44109961_44109962insTCATT	GRCh37
NC_000017.9:g.41465808_41465809insTCATT	NCBI36
NG_032784.1:g.197779_197780insAATGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.2838-297_2838-296insAATGA MANE Select	ENSP00000387393.3:n.2838-297_2838-296insAATGA
ENST00000572904.6:c.2838-297_2838-296insAATGA	ENSP00000461484.1:n.2838-297_2838-296insAATGA
ENST00000574590.6:c.2835-297_2835-296insAATGA	ENSP00000461812.2:n.2835-297_2835-296insAATGA
ENST00000575318.6:c.2646-297_2646-296insAATGA	ENSP00000461299.1:n.2646-297_2646-296insAATGA
ENST00000638275.1:c.2646-297_2646-296insAATGA	ENSP00000492576.1:n.2646-297_2646-296insAATGA
ENST00000638291.1:n.666-297_666-296insAATGA
ENST00000638551.1:n.786-297_786-296insAATGA
ENST00000639467.1:c.495-297_495-296insAATGA	ENSP00000492741.1:n.495-297_495-296insAATGA
ENST00000639531.1:c.2649-297_2649-296insAATGA	ENSP00000491765.1:n.2649-297_2649-296insAATGA
ENST00000639805.1:n.255-297_255-296insAATGA
ENST00000640092.1:n.1525-297_1525-296insAATGA
ENST00000640751.1:n.433-297_433-296insAATGA
ENST00000648792.1:c.2838-429_2838-428insAATGA	ENSP00000497628.1:n.2838-429_2838-428insAATGA
ENST00000262419.10:c.2838-297_2838-296insAATGA	ENSP00000262419.6:n.2838-297_2838-296insAATGA
ENST00000432791.5:c.2835-297_2835-296insAATGA	ENSP00000387393.2:n.2835-297_2835-296insAATGA
ENST00000572218.5:n.7055-297_7055-296insAATGA
ENST00000572904.5:c.2838-297_2838-296insAATGA	ENSP00000461484.1:n.2838-297_2838-296insAATGA
ENST00000573682.1:n.224-297_224-296insAATGA
ENST00000574590.5:c.2838-297_2838-296insAATGA	ENSP00000461812.1:n.2838-297_2838-296insAATGA
ENST00000575318.5:c.2646-297_2646-296insAATGA	ENSP00000461299.1:n.2646-297_2646-296insAATGA
ENST00000576870.5:n.810-297_810-296insAATGA
NM_001193465.1:c.2835-297_2835-296insAATGA	NP_001180394.1:n.2835-297_2835-296insAATGA
NM_001193466.1:c.2838-297_2838-296insAATGA	NP_001180395.1:n.2838-297_2838-296insAATGA
NM_015443.3:c.2838-297_2838-296insAATGA	NP_056258.1:n.2838-297_2838-296insAATGA
XM_006721823.1:c.2838-297_2838-296insAATGA	XP_006721886.1:n.2838-297_2838-296insAATGA
XM_006721824.2:c.2838-297_2838-296insAATGA	XP_006721887.1:n.2838-297_2838-296insAATGA
XM_011524628.1:c.2835-297_2835-296insAATGA	XP_011522930.1:n.2835-297_2835-296insAATGA
XM_011524629.1:c.2736-297_2736-296insAATGA	XP_011522931.1:n.2736-297_2736-296insAATGA
XM_011524630.1:c.2649-297_2649-296insAATGA	XP_011522932.1:n.2649-297_2649-296insAATGA
XM_011524631.1:c.2646-297_2646-296insAATGA	XP_011522933.1:n.2646-297_2646-296insAATGA
XM_011524632.1:c.1608-297_1608-296insAATGA	XP_011522934.1:n.1608-297_1608-296insAATGA
XM_006721823.2:c.2838-297_2838-296insAATGA	XP_006721886.1:n.2838-297_2838-296insAATGA
XM_006721824.4:c.2838-297_2838-296insAATGA	XP_006721887.1:n.2838-297_2838-296insAATGA
XM_011524628.3:c.2835-297_2835-296insAATGA	XP_011522930.1:n.2835-297_2835-296insAATGA
XM_011524629.3:c.2736-297_2736-296insAATGA	XP_011522931.1:n.2736-297_2736-296insAATGA
XM_011524630.3:c.2649-297_2649-296insAATGA	XP_011522932.1:n.2649-297_2649-296insAATGA
XM_011524631.3:c.2646-297_2646-296insAATGA	XP_011522933.1:n.2646-297_2646-296insAATGA
XM_011524632.3:c.1608-297_1608-296insAATGA	XP_011522934.1:n.1608-297_1608-296insAATGA
XM_017024488.2:c.2646-297_2646-296insAATGA	XP_016879977.1:n.2646-297_2646-296insAATGA
NM_001193466.2:c.2838-297_2838-296insAATGA	NP_001180395.1:n.2838-297_2838-296insAATGA
NM_015443.4:c.2838-297_2838-296insAATGA MANE Select	NP_056258.1:n.2838-297_2838-296insAATGA
NM_001193465.2:c.2835-297_2835-296insAATGA	NP_001180394.1:n.2835-297_2835-296insAATGA
NM_001379198.1:c.2838-297_2838-296insAATGA	NP_001366127.1:n.2838-297_2838-296insAATGA