Canonical Allele Identifier: CA2638386612

Gene: KANSL1

Linked Data

• gnomAD v4: 17-46193201-T-TCAG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46193202_46193203insAGC , CM000679.2:g.46193202_46193203insAGC	GRCh38
NC_000017.10:g.44270568_44270569insAGC , CM000679.1:g.44270568_44270569insAGC	GRCh37
NC_000017.9:g.41626345_41626346insAGC	NCBI36
NG_032784.1:g.37173_37174insCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.-469_-468insCTG MANE Select	ENSP00000387393.3:n.-469_-468insCTG
ENST00000571698.2:c.-90+548_-90+549insCTG	ENSP00000459330.2:n.-90+548_-90+549insCTG
ENST00000572904.6:c.-89-20970_-89-20969insCTG	ENSP00000461484.1:n.-89-20970_-89-20969insCTG
ENST00000574590.6:c.-89-20970_-89-20969insCTG	ENSP00000461812.2:n.-89-20970_-89-20969insCTG
ENST00000574655.6:n.166-20970_166-20969insCTG
ENST00000575318.6:c.-89-20970_-89-20969insCTG	ENSP00000461299.1:n.-89-20970_-89-20969insCTG
ENST00000576739.2:c.-89-20970_-89-20969insCTG	ENSP00000459627.1:n.-89-20970_-89-20969insCTG
ENST00000638269.1:n.156-20970_156-20969insCTG
ENST00000638275.1:c.-469_-468insCTG	ENSP00000492576.1:n.-469_-468insCTG
ENST00000638902.1:n.16-20970_16-20969insCTG
ENST00000639099.1:n.162-20970_162-20969insCTG
ENST00000639150.1:c.23+30469_23+30470insCTG	ENSP00000491906.1:n.23+30469_23+30470insCTG
ENST00000639356.1:n.162-20970_162-20969insCTG
ENST00000639375.1:n.150-20970_150-20969insCTG
ENST00000648792.1:c.-89-20970_-89-20969insCTG	ENSP00000497628.1:n.-89-20970_-89-20969insCTG
ENST00000432791.5:c.-89-20970_-89-20969insCTG	ENSP00000387393.2:n.-89-20970_-89-20969insCTG
ENST00000571698.1:c.-90+548_-90+549insCTG	ENSP00000459330.1:n.-90+548_-90+549insCTG
ENST00000574590.5:c.-89-20970_-89-20969insCTG	ENSP00000461812.1:n.-89-20970_-89-20969insCTG
ENST00000574655.5:c.-89-20970_-89-20969insCTG	ENSP00000459359.1:n.-89-20970_-89-20969insCTG
ENST00000576739.1:c.-89-20970_-89-20969insCTG	ENSP00000459627.1:n.-89-20970_-89-20969insCTG
NM_001193465.1:c.-89-20970_-89-20969insCTG	NP_001180394.1:n.-89-20970_-89-20969insCTG
XM_006721823.1:c.-89-20970_-89-20969insCTG	XP_006721886.1:n.-89-20970_-89-20969insCTG
XM_006721824.2:c.-89-20970_-89-20969insCTG	XP_006721887.1:n.-89-20970_-89-20969insCTG
XM_011524628.1:c.-89-20970_-89-20969insCTG	XP_011522930.1:n.-89-20970_-89-20969insCTG
XM_011524629.1:c.-89-20970_-89-20969insCTG	XP_011522931.1:n.-89-20970_-89-20969insCTG
XM_011524630.1:c.-89-20970_-89-20969insCTG	XP_011522932.1:n.-89-20970_-89-20969insCTG
XM_011524631.1:c.-89-20970_-89-20969insCTG	XP_011522933.1:n.-89-20970_-89-20969insCTG
XM_006721823.2:c.-89-20970_-89-20969insCTG	XP_006721886.1:n.-89-20970_-89-20969insCTG
XM_006721824.4:c.-89-20970_-89-20969insCTG	XP_006721887.1:n.-89-20970_-89-20969insCTG
XM_011524628.3:c.-89-20970_-89-20969insCTG	XP_011522930.1:n.-89-20970_-89-20969insCTG
XM_011524629.3:c.-89-20970_-89-20969insCTG	XP_011522931.1:n.-89-20970_-89-20969insCTG
XM_011524630.3:c.-89-20970_-89-20969insCTG	XP_011522932.1:n.-89-20970_-89-20969insCTG
XM_011524631.3:c.-89-20970_-89-20969insCTG	XP_011522933.1:n.-89-20970_-89-20969insCTG
XM_017024488.2:c.-89-20970_-89-20969insCTG	XP_016879977.1:n.-89-20970_-89-20969insCTG
NM_015443.4:c.-469_-468insCTG MANE Select	NP_056258.1:n.-469_-468insCTG
NM_001193465.2:c.-89-20970_-89-20969insCTG	NP_001180394.1:n.-89-20970_-89-20969insCTG
NM_001379198.1:c.-89-20970_-89-20969insCTG	NP_001366127.1:n.-89-20970_-89-20969insCTG