Canonical Allele Identifier: CA2262110634

Gene: KANSL1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46031333_46031335delinsAAT , CM000679.2:g.46031333_46031335delinsAAT	GRCh38
NC_000017.10:g.44108699_44108701delinsAAT , CM000679.1:g.44108699_44108701delinsAAT	GRCh37
NC_000017.9:g.41464546_41464548delinsAAT	NCBI36
NG_032784.1:g.199040_199042delinsATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.*141_*143delinsATT MANE Select	ENSP00000387393.3:n.*141_*143delinsATT
ENST00000572904.6:c.*141_*143delinsATT	ENSP00000461484.1:n.*141_*143delinsATT
ENST00000574590.6:c.*141_*143delinsATT	ENSP00000461812.2:n.*141_*143delinsATT
ENST00000575318.6:c.*141_*143delinsATT	ENSP00000461299.1:n.*141_*143delinsATT
ENST00000638275.1:c.*141_*143delinsATT	ENSP00000492576.1:n.*141_*143delinsATT
ENST00000648792.1:c.*141_*143delinsATT	ENSP00000497628.1:n.*141_*143delinsATT
ENST00000262419.10:c.*141_*143delinsATT	ENSP00000262419.6:n.*141_*143delinsATT
ENST00000432791.5:c.*141_*143delinsATT	ENSP00000387393.2:n.*141_*143delinsATT
ENST00000572218.5:n.7676_7678delinsATT
ENST00000572904.5:c.*141_*143delinsATT	ENSP00000461484.1:n.*141_*143delinsATT
ENST00000574590.5:c.*141_*143delinsATT	ENSP00000461812.1:n.*141_*143delinsATT
ENST00000574963.1:n.1232_1234delinsATT
ENST00000575318.5:c.*141_*143delinsATT	ENSP00000461299.1:n.*141_*143delinsATT
ENST00000576870.5:n.1431_1433delinsATT
NM_001193465.1:c.*141_*143delinsATT	NP_001180394.1:n.*141_*143delinsATT
NM_001193466.1:c.*141_*143delinsATT	NP_001180395.1:n.*141_*143delinsATT
NM_015443.3:c.*141_*143delinsATT	NP_056258.1:n.*141_*143delinsATT
XM_006721823.1:c.*141_*143delinsATT	XP_006721886.1:n.*141_*143delinsATT
XM_006721824.2:c.*141_*143delinsATT	XP_006721887.1:n.*141_*143delinsATT
XM_011524628.1:c.*141_*143delinsATT	XP_011522930.1:n.*141_*143delinsATT
XM_011524629.1:c.*141_*143delinsATT	XP_011522931.1:n.*141_*143delinsATT
XM_011524630.1:c.*141_*143delinsATT	XP_011522932.1:n.*141_*143delinsATT
XM_011524631.1:c.*141_*143delinsATT	XP_011522933.1:n.*141_*143delinsATT
XM_011524632.1:c.*141_*143delinsATT	XP_011522934.1:n.*141_*143delinsATT
XM_006721823.2:c.*141_*143delinsATT	XP_006721886.1:n.*141_*143delinsATT
XM_006721824.4:c.*141_*143delinsATT	XP_006721887.1:n.*141_*143delinsATT
XM_011524628.3:c.*141_*143delinsATT	XP_011522930.1:n.*141_*143delinsATT
XM_011524629.3:c.*141_*143delinsATT	XP_011522931.1:n.*141_*143delinsATT
XM_011524630.3:c.*141_*143delinsATT	XP_011522932.1:n.*141_*143delinsATT
XM_011524631.3:c.*141_*143delinsATT	XP_011522933.1:n.*141_*143delinsATT
XM_011524632.3:c.*141_*143delinsATT	XP_011522934.1:n.*141_*143delinsATT
XM_017024488.2:c.*141_*143delinsATT	XP_016879977.1:n.*141_*143delinsATT
NM_001193466.2:c.*141_*143delinsATT	NP_001180395.1:n.*141_*143delinsATT
NM_015443.4:c.*141_*143delinsATT MANE Select	NP_056258.1:n.*141_*143delinsATT
NM_001193465.2:c.*141_*143delinsATT	NP_001180394.1:n.*141_*143delinsATT
NM_001379198.1:c.*141_*143delinsATT	NP_001366127.1:n.*141_*143delinsATT