Canonical Allele Identifier: CA2638373442

Gene: KANSL1

Linked Data

• gnomAD v4: 17-46032590-CAAAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46032594_46032597del , CM000679.2:g.46032594_46032597del	GRCh38
NC_000017.10:g.44109960_44109963del , CM000679.1:g.44109960_44109963del	GRCh37
NC_000017.9:g.41465807_41465810del	NCBI36
NG_032784.1:g.197781_197784del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.2838-295_2838-292del MANE Select	ENSP00000387393.3:n.2838-295_2838-292del
ENST00000572904.6:c.2838-295_2838-292del	ENSP00000461484.1:n.2838-295_2838-292del
ENST00000574590.6:c.2835-295_2835-292del	ENSP00000461812.2:n.2835-295_2835-292del
ENST00000575318.6:c.2646-295_2646-292del	ENSP00000461299.1:n.2646-295_2646-292del
ENST00000638275.1:c.2646-295_2646-292del	ENSP00000492576.1:n.2646-295_2646-292del
ENST00000638291.1:n.666-295_666-292del
ENST00000638551.1:n.786-295_786-292del
ENST00000639467.1:c.495-295_495-292del	ENSP00000492741.1:n.495-295_495-292del
ENST00000639531.1:c.2649-295_2649-292del	ENSP00000491765.1:n.2649-295_2649-292del
ENST00000639805.1:n.255-295_255-292del
ENST00000640092.1:n.1525-295_1525-292del
ENST00000640751.1:n.433-295_433-292del
ENST00000648792.1:c.2838-427_2838-424del	ENSP00000497628.1:n.2838-427_2838-424del
ENST00000262419.10:c.2838-295_2838-292del	ENSP00000262419.6:n.2838-295_2838-292del
ENST00000432791.5:c.2835-295_2835-292del	ENSP00000387393.2:n.2835-295_2835-292del
ENST00000572218.5:n.7055-295_7055-292del
ENST00000572904.5:c.2838-295_2838-292del	ENSP00000461484.1:n.2838-295_2838-292del
ENST00000573682.1:n.224-295_224-292del
ENST00000574590.5:c.2838-295_2838-292del	ENSP00000461812.1:n.2838-295_2838-292del
ENST00000575318.5:c.2646-295_2646-292del	ENSP00000461299.1:n.2646-295_2646-292del
ENST00000576870.5:n.810-295_810-292del
NM_001193465.1:c.2835-295_2835-292del	NP_001180394.1:n.2835-295_2835-292del
NM_001193466.1:c.2838-295_2838-292del	NP_001180395.1:n.2838-295_2838-292del
NM_015443.3:c.2838-295_2838-292del	NP_056258.1:n.2838-295_2838-292del
XM_006721823.1:c.2838-295_2838-292del	XP_006721886.1:n.2838-295_2838-292del
XM_006721824.2:c.2838-295_2838-292del	XP_006721887.1:n.2838-295_2838-292del
XM_011524628.1:c.2835-295_2835-292del	XP_011522930.1:n.2835-295_2835-292del
XM_011524629.1:c.2736-295_2736-292del	XP_011522931.1:n.2736-295_2736-292del
XM_011524630.1:c.2649-295_2649-292del	XP_011522932.1:n.2649-295_2649-292del
XM_011524631.1:c.2646-295_2646-292del	XP_011522933.1:n.2646-295_2646-292del
XM_011524632.1:c.1608-295_1608-292del	XP_011522934.1:n.1608-295_1608-292del
XM_006721823.2:c.2838-295_2838-292del	XP_006721886.1:n.2838-295_2838-292del
XM_006721824.4:c.2838-295_2838-292del	XP_006721887.1:n.2838-295_2838-292del
XM_011524628.3:c.2835-295_2835-292del	XP_011522930.1:n.2835-295_2835-292del
XM_011524629.3:c.2736-295_2736-292del	XP_011522931.1:n.2736-295_2736-292del
XM_011524630.3:c.2649-295_2649-292del	XP_011522932.1:n.2649-295_2649-292del
XM_011524631.3:c.2646-295_2646-292del	XP_011522933.1:n.2646-295_2646-292del
XM_011524632.3:c.1608-295_1608-292del	XP_011522934.1:n.1608-295_1608-292del
XM_017024488.2:c.2646-295_2646-292del	XP_016879977.1:n.2646-295_2646-292del
NM_001193466.2:c.2838-295_2838-292del	NP_001180395.1:n.2838-295_2838-292del
NM_015443.4:c.2838-295_2838-292del MANE Select	NP_056258.1:n.2838-295_2838-292del
NM_001193465.2:c.2835-295_2835-292del	NP_001180394.1:n.2835-295_2835-292del
NM_001379198.1:c.2838-295_2838-292del	NP_001366127.1:n.2838-295_2838-292del