Canonical Allele Identifier: CA2262111205

Gene: KANSL1

Linked Data

• dbSNP Id: rs2077040868

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46032576_46032577del , CM000679.2:g.46032576_46032577del	GRCh38
NC_000017.10:g.44109942_44109943del , CM000679.1:g.44109942_44109943del	GRCh37
NC_000017.9:g.41465789_41465790del	NCBI36
NG_032784.1:g.197799_197800del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.2838-277_2838-276del MANE Select	ENSP00000387393.3:n.2838-277_2838-276del
ENST00000572904.6:c.2838-277_2838-276del	ENSP00000461484.1:n.2838-277_2838-276del
ENST00000574590.6:c.2835-277_2835-276del	ENSP00000461812.2:n.2835-277_2835-276del
ENST00000575318.6:c.2646-277_2646-276del	ENSP00000461299.1:n.2646-277_2646-276del
ENST00000638275.1:c.2646-277_2646-276del	ENSP00000492576.1:n.2646-277_2646-276del
ENST00000638291.1:n.666-277_666-276del
ENST00000638551.1:n.786-277_786-276del
ENST00000639467.1:c.495-277_495-276del	ENSP00000492741.1:n.495-277_495-276del
ENST00000639531.1:c.2649-277_2649-276del	ENSP00000491765.1:n.2649-277_2649-276del
ENST00000639805.1:n.255-277_255-276del
ENST00000640092.1:n.1525-277_1525-276del
ENST00000640751.1:n.433-277_433-276del
ENST00000648792.1:c.2838-409_2838-408del	ENSP00000497628.1:n.2838-409_2838-408del
ENST00000262419.10:c.2838-277_2838-276del	ENSP00000262419.6:n.2838-277_2838-276del
ENST00000432791.5:c.2835-277_2835-276del	ENSP00000387393.2:n.2835-277_2835-276del
ENST00000572218.5:n.7055-277_7055-276del
ENST00000572904.5:c.2838-277_2838-276del	ENSP00000461484.1:n.2838-277_2838-276del
ENST00000573682.1:n.224-277_224-276del
ENST00000574590.5:c.2838-277_2838-276del	ENSP00000461812.1:n.2838-277_2838-276del
ENST00000575318.5:c.2646-277_2646-276del	ENSP00000461299.1:n.2646-277_2646-276del
ENST00000576870.5:n.810-277_810-276del
NM_001193465.1:c.2835-277_2835-276del	NP_001180394.1:n.2835-277_2835-276del
NM_001193466.1:c.2838-277_2838-276del	NP_001180395.1:n.2838-277_2838-276del
NM_015443.3:c.2838-277_2838-276del	NP_056258.1:n.2838-277_2838-276del
XM_006721823.1:c.2838-277_2838-276del	XP_006721886.1:n.2838-277_2838-276del
XM_006721824.2:c.2838-277_2838-276del	XP_006721887.1:n.2838-277_2838-276del
XM_011524628.1:c.2835-277_2835-276del	XP_011522930.1:n.2835-277_2835-276del
XM_011524629.1:c.2736-277_2736-276del	XP_011522931.1:n.2736-277_2736-276del
XM_011524630.1:c.2649-277_2649-276del	XP_011522932.1:n.2649-277_2649-276del
XM_011524631.1:c.2646-277_2646-276del	XP_011522933.1:n.2646-277_2646-276del
XM_011524632.1:c.1608-277_1608-276del	XP_011522934.1:n.1608-277_1608-276del
XM_006721823.2:c.2838-277_2838-276del	XP_006721886.1:n.2838-277_2838-276del
XM_006721824.4:c.2838-277_2838-276del	XP_006721887.1:n.2838-277_2838-276del
XM_011524628.3:c.2835-277_2835-276del	XP_011522930.1:n.2835-277_2835-276del
XM_011524629.3:c.2736-277_2736-276del	XP_011522931.1:n.2736-277_2736-276del
XM_011524630.3:c.2649-277_2649-276del	XP_011522932.1:n.2649-277_2649-276del
XM_011524631.3:c.2646-277_2646-276del	XP_011522933.1:n.2646-277_2646-276del
XM_011524632.3:c.1608-277_1608-276del	XP_011522934.1:n.1608-277_1608-276del
XM_017024488.2:c.2646-277_2646-276del	XP_016879977.1:n.2646-277_2646-276del
NM_001193466.2:c.2838-277_2838-276del	NP_001180395.1:n.2838-277_2838-276del
NM_015443.4:c.2838-277_2838-276del MANE Select	NP_056258.1:n.2838-277_2838-276del
NM_001193465.2:c.2835-277_2835-276del	NP_001180394.1:n.2835-277_2835-276del
NM_001379198.1:c.2838-277_2838-276del	NP_001366127.1:n.2838-277_2838-276del