Canonical Allele Identifier: CA2262127340

Gene: KANSL1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46066494_46066495delinsCT , CM000679.2:g.46066494_46066495delinsCT	GRCh38
NC_000017.10:g.44143860_44143861delinsCT , CM000679.1:g.44143860_44143861delinsCT	GRCh37
NC_000017.9:g.41499682_41499683delinsCT	NCBI36
NG_032784.1:g.163880_163881delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.1848+42_1848+43delinsAG MANE Select	ENSP00000387393.3:n.1848+42_1848+43delinsAG
ENST00000571698.2:c.1848+42_1848+43delinsAG	ENSP00000459330.2:n.1848+42_1848+43delinsAG
ENST00000572904.6:c.1848+42_1848+43delinsAG	ENSP00000461484.1:n.1848+42_1848+43delinsAG
ENST00000574590.6:c.1848+42_1848+43delinsAG	ENSP00000461812.2:n.1848+42_1848+43delinsAG
ENST00000575318.6:c.1848+42_1848+43delinsAG	ENSP00000461299.1:n.1848+42_1848+43delinsAG
ENST00000577114.2:n.574+42_574+43delinsAG
ENST00000638275.1:c.1848+42_1848+43delinsAG	ENSP00000492576.1:n.1848+42_1848+43delinsAG
ENST00000639150.1:c.582+42_582+43delinsAG	ENSP00000491906.1:n.582+42_582+43delinsAG
ENST00000639375.1:n.2086+42_2086+43delinsAG
ENST00000639531.1:c.1848+42_1848+43delinsAG	ENSP00000491765.1:n.1848+42_1848+43delinsAG
ENST00000639853.1:c.1019+42_1019+43delinsAG
ENST00000648792.1:c.1848+42_1848+43delinsAG	ENSP00000497628.1:n.1848+42_1848+43delinsAG
ENST00000262419.10:c.1848+42_1848+43delinsAG	ENSP00000262419.6:n.1848+42_1848+43delinsAG
ENST00000432791.5:c.1848+42_1848+43delinsAG	ENSP00000387393.2:n.1848+42_1848+43delinsAG
ENST00000572904.5:c.1848+42_1848+43delinsAG	ENSP00000461484.1:n.1848+42_1848+43delinsAG
ENST00000574590.5:c.1848+42_1848+43delinsAG	ENSP00000461812.1:n.1848+42_1848+43delinsAG
ENST00000575318.5:c.1848+42_1848+43delinsAG	ENSP00000461299.1:n.1848+42_1848+43delinsAG
ENST00000577114.1:n.645+42_645+43delinsAG
NM_001193465.1:c.1848+42_1848+43delinsAG	NP_001180394.1:n.1848+42_1848+43delinsAG
NM_001193466.1:c.1848+42_1848+43delinsAG	NP_001180395.1:n.1848+42_1848+43delinsAG
NM_015443.3:c.1848+42_1848+43delinsAG	NP_056258.1:n.1848+42_1848+43delinsAG
XM_006721823.1:c.1848+42_1848+43delinsAG	XP_006721886.1:n.1848+42_1848+43delinsAG
XM_006721824.2:c.1848+42_1848+43delinsAG	XP_006721887.1:n.1848+42_1848+43delinsAG
XM_011524628.1:c.1848+42_1848+43delinsAG	XP_011522930.1:n.1848+42_1848+43delinsAG
XM_011524629.1:c.1746+42_1746+43delinsAG	XP_011522931.1:n.1746+42_1746+43delinsAG
XM_011524630.1:c.1848+42_1848+43delinsAG	XP_011522932.1:n.1848+42_1848+43delinsAG
XM_011524631.1:c.1848+42_1848+43delinsAG	XP_011522933.1:n.1848+42_1848+43delinsAG
XM_011524632.1:c.618+42_618+43delinsAG	XP_011522934.1:n.618+42_618+43delinsAG
XM_006721823.2:c.1848+42_1848+43delinsAG	XP_006721886.1:n.1848+42_1848+43delinsAG
XM_006721824.4:c.1848+42_1848+43delinsAG	XP_006721887.1:n.1848+42_1848+43delinsAG
XM_011524628.3:c.1848+42_1848+43delinsAG	XP_011522930.1:n.1848+42_1848+43delinsAG
XM_011524629.3:c.1746+42_1746+43delinsAG	XP_011522931.1:n.1746+42_1746+43delinsAG
XM_011524630.3:c.1848+42_1848+43delinsAG	XP_011522932.1:n.1848+42_1848+43delinsAG
XM_011524631.3:c.1848+42_1848+43delinsAG	XP_011522933.1:n.1848+42_1848+43delinsAG
XM_011524632.3:c.618+42_618+43delinsAG	XP_011522934.1:n.618+42_618+43delinsAG
XM_017024488.2:c.1848+42_1848+43delinsAG	XP_016879977.1:n.1848+42_1848+43delinsAG
XM_017024489.1:c.1746+42_1746+43delinsAG	XP_016879978.1:n.1746+42_1746+43delinsAG
NM_001193466.2:c.1848+42_1848+43delinsAG	NP_001180395.1:n.1848+42_1848+43delinsAG
NM_015443.4:c.1848+42_1848+43delinsAG MANE Select	NP_056258.1:n.1848+42_1848+43delinsAG
NM_001193465.2:c.1848+42_1848+43delinsAG	NP_001180394.1:n.1848+42_1848+43delinsAG
NM_001379198.1:c.1848+42_1848+43delinsAG	NP_001366127.1:n.1848+42_1848+43delinsAG