Canonical Allele Identifier: CA2262110491

Gene: KANSL1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46031050_46031051delinsAG , CM000679.2:g.46031050_46031051delinsAG	GRCh38
NC_000017.10:g.44108416_44108417delinsAG , CM000679.1:g.44108416_44108417delinsAG	GRCh37
NC_000017.9:g.41464263_41464264delinsAG	NCBI36
NG_032784.1:g.199324_199325delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.*425_*426delinsCT MANE Select	ENSP00000387393.3:n.*425_*426delinsCT
ENST00000572904.6:c.*425_*426delinsCT	ENSP00000461484.1:n.*425_*426delinsCT
ENST00000574590.6:c.*425_*426delinsCT	ENSP00000461812.2:n.*425_*426delinsCT
ENST00000575318.6:c.*425_*426delinsCT	ENSP00000461299.1:n.*425_*426delinsCT
ENST00000638275.1:c.*425_*426delinsCT	ENSP00000492576.1:n.*425_*426delinsCT
ENST00000648792.1:c.*425_*426delinsCT	ENSP00000497628.1:n.*425_*426delinsCT
ENST00000262419.10:c.*425_*426delinsCT	ENSP00000262419.6:n.*425_*426delinsCT
ENST00000432791.5:c.*425_*426delinsCT	ENSP00000387393.2:n.*425_*426delinsCT
ENST00000572218.5:n.7960_7961delinsCT
ENST00000572904.5:c.*425_*426delinsCT	ENSP00000461484.1:n.*425_*426delinsCT
ENST00000574590.5:c.*425_*426delinsCT	ENSP00000461812.1:n.*425_*426delinsCT
ENST00000575318.5:c.*425_*426delinsCT	ENSP00000461299.1:n.*425_*426delinsCT
ENST00000576870.5:n.1715_1716delinsCT
NM_001193465.1:c.*425_*426delinsCT	NP_001180394.1:n.*425_*426delinsCT
NM_001193466.1:c.*425_*426delinsCT	NP_001180395.1:n.*425_*426delinsCT
NM_015443.3:c.*425_*426delinsCT	NP_056258.1:n.*425_*426delinsCT
XM_006721823.1:c.*425_*426delinsCT	XP_006721886.1:n.*425_*426delinsCT
XM_006721824.2:c.*425_*426delinsCT	XP_006721887.1:n.*425_*426delinsCT
XM_011524628.1:c.*425_*426delinsCT	XP_011522930.1:n.*425_*426delinsCT
XM_011524629.1:c.*425_*426delinsCT	XP_011522931.1:n.*425_*426delinsCT
XM_011524630.1:c.*425_*426delinsCT	XP_011522932.1:n.*425_*426delinsCT
XM_011524631.1:c.*425_*426delinsCT	XP_011522933.1:n.*425_*426delinsCT
XM_011524632.1:c.*425_*426delinsCT	XP_011522934.1:n.*425_*426delinsCT
XM_006721823.2:c.*425_*426delinsCT	XP_006721886.1:n.*425_*426delinsCT
XM_006721824.4:c.*425_*426delinsCT	XP_006721887.1:n.*425_*426delinsCT
XM_011524628.3:c.*425_*426delinsCT	XP_011522930.1:n.*425_*426delinsCT
XM_011524629.3:c.*425_*426delinsCT	XP_011522931.1:n.*425_*426delinsCT
XM_011524630.3:c.*425_*426delinsCT	XP_011522932.1:n.*425_*426delinsCT
XM_011524631.3:c.*425_*426delinsCT	XP_011522933.1:n.*425_*426delinsCT
XM_011524632.3:c.*425_*426delinsCT	XP_011522934.1:n.*425_*426delinsCT
XM_017024488.2:c.*425_*426delinsCT	XP_016879977.1:n.*425_*426delinsCT
NM_001193466.2:c.*425_*426delinsCT	NP_001180395.1:n.*425_*426delinsCT
NM_015443.4:c.*425_*426delinsCT MANE Select	NP_056258.1:n.*425_*426delinsCT
NM_001193465.2:c.*425_*426delinsCT	NP_001180394.1:n.*425_*426delinsCT
NM_001379198.1:c.*425_*426delinsCT	NP_001366127.1:n.*425_*426delinsCT