Canonical Allele Identifier: CA2262110699

Gene: KANSL1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46031480_46031482delinsCTG , CM000679.2:g.46031480_46031482delinsCTG	GRCh38
NC_000017.10:g.44108846_44108848delinsCTG , CM000679.1:g.44108846_44108848delinsCTG	GRCh37
NC_000017.9:g.41464693_41464695delinsCTG	NCBI36
NG_032784.1:g.198893_198895delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.3312_3314delinsCAG MANE Select	ENSP00000387393.3:p.His1104=
ENST00000572904.6:c.3312_3314delinsCAG	ENSP00000461484.1:p.His1104=
ENST00000574590.6:c.3309_3311delinsCAG	ENSP00000461812.2:p.His1103=
ENST00000575318.6:c.3120_3122delinsCAG	ENSP00000461299.1:p.His1040=
ENST00000638275.1:c.3120_3122delinsCAG	ENSP00000492576.1:p.His1040=
ENST00000648792.1:c.3180_3182delinsCAG	ENSP00000497628.1:p.His1060=
ENST00000262419.10:c.3312_3314delinsCAG	ENSP00000262419.6:p.His1104=
ENST00000432791.5:c.3309_3311delinsCAG	ENSP00000387393.2:p.His1103=
ENST00000572218.5:n.7529_7531delinsCAG
ENST00000572904.5:c.3312_3314delinsCAG	ENSP00000461484.1:p.His1104=
ENST00000574590.5:c.3312_3314delinsCAG	ENSP00000461812.1:p.His1104=
ENST00000574963.1:n.1085_1087delinsCAG
ENST00000575318.5:c.3120_3122delinsCAG	ENSP00000461299.1:p.His1040=
ENST00000576870.5:n.1284_1286delinsCAG
NM_001193465.1:c.3309_3311delinsCAG	NP_001180394.1:p.His1103=
NM_001193466.1:c.3312_3314delinsCAG	NP_001180395.1:p.His1104=
NM_015443.3:c.3312_3314delinsCAG	NP_056258.1:p.His1104=
XM_006721823.1:c.3312_3314delinsCAG	XP_006721886.1:p.His1104=
XM_006721824.2:c.3312_3314delinsCAG	XP_006721887.1:p.His1104=
XM_011524628.1:c.3309_3311delinsCAG	XP_011522930.1:p.His1103=
XM_011524629.1:c.3210_3212delinsCAG	XP_011522931.1:p.His1070=
XM_011524630.1:c.3123_3125delinsCAG	XP_011522932.1:p.His1041=
XM_011524631.1:c.3120_3122delinsCAG	XP_011522933.1:p.His1040=
XM_011524632.1:c.2082_2084delinsCAG	XP_011522934.1:p.His694=
XM_006721823.2:c.3312_3314delinsCAG	XP_006721886.1:p.His1104=
XM_006721824.4:c.3312_3314delinsCAG	XP_006721887.1:p.His1104=
XM_011524628.3:c.3309_3311delinsCAG	XP_011522930.1:p.His1103=
XM_011524629.3:c.3210_3212delinsCAG	XP_011522931.1:p.His1070=
XM_011524630.3:c.3123_3125delinsCAG	XP_011522932.1:p.His1041=
XM_011524631.3:c.3120_3122delinsCAG	XP_011522933.1:p.His1040=
XM_011524632.3:c.2082_2084delinsCAG	XP_011522934.1:p.His694=
XM_017024488.2:c.3120_3122delinsCAG	XP_016879977.1:p.His1040=
NM_001193466.2:c.3312_3314delinsCAG	NP_001180395.1:p.His1104=
NM_015443.4:c.3312_3314delinsCAG MANE Select	NP_056258.1:p.His1104=
NM_001193465.2:c.3309_3311delinsCAG	NP_001180394.1:p.His1103=
NM_001379198.1:c.3312_3314delinsCAG	NP_001366127.1:p.His1104=