Canonical Allele Identifier: CA2262180034

Gene: KANSL1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46171445_46171448delinsAGAG , CM000679.2:g.46171445_46171448delinsAGAG	GRCh38
NC_000017.10:g.44248811_44248814delinsAGAG , CM000679.1:g.44248811_44248814delinsAGAG	GRCh37
NC_000017.9:g.41604588_41604591delinsAGAG	NCBI36
NG_032784.1:g.58927_58930delinsCTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.696_699delinsCTCT MANE Select	ENSP00000387393.3:p.Ser232=
ENST00000571698.2:c.696_699delinsCTCT	ENSP00000459330.2:p.Ser232=
ENST00000572904.6:c.696_699delinsCTCT	ENSP00000461484.1:p.Ser232=
ENST00000574590.6:c.696_699delinsCTCT	ENSP00000461812.2:p.Ser232=
ENST00000574655.6:n.950_953delinsCTCT
ENST00000575318.6:c.696_699delinsCTCT	ENSP00000461299.1:p.Ser232=
ENST00000638269.1:n.940_943delinsCTCT
ENST00000638275.1:c.696_699delinsCTCT	ENSP00000492576.1:p.Ser232=
ENST00000638902.1:n.800_803delinsCTCT
ENST00000639099.1:n.946_949delinsCTCT
ENST00000639150.1:c.23+52223_23+52226delinsCTCT	ENSP00000491906.1:n.23+52223_23+52226delinsCTCT
ENST00000639356.1:n.946_949delinsCTCT
ENST00000639375.1:n.934_937delinsCTCT
ENST00000639531.1:c.696_699delinsCTCT	ENSP00000491765.1:p.Ser232=
ENST00000648792.1:c.696_699delinsCTCT	ENSP00000497628.1:p.Ser232=
ENST00000262419.10:c.696_699delinsCTCT	ENSP00000262419.6:p.Ser232=
ENST00000432791.5:c.696_699delinsCTCT	ENSP00000387393.2:p.Ser232=
ENST00000572904.5:c.696_699delinsCTCT	ENSP00000461484.1:p.Ser232=
ENST00000574590.5:c.696_699delinsCTCT	ENSP00000461812.1:p.Ser232=
ENST00000575318.5:c.696_699delinsCTCT	ENSP00000461299.1:p.Ser232=
NM_001193465.1:c.696_699delinsCTCT	NP_001180394.1:p.Ser232=
NM_001193466.1:c.696_699delinsCTCT	NP_001180395.1:p.Ser232=
NM_015443.3:c.696_699delinsCTCT	NP_056258.1:p.Ser232=
XM_006721823.1:c.696_699delinsCTCT	XP_006721886.1:p.Ser232=
XM_006721824.2:c.696_699delinsCTCT	XP_006721887.1:p.Ser232=
XM_011524628.1:c.696_699delinsCTCT	XP_011522930.1:p.Ser232=
XM_011524629.1:c.696_699delinsCTCT	XP_011522931.1:p.Ser232=
XM_011524630.1:c.696_699delinsCTCT	XP_011522932.1:p.Ser232=
XM_011524631.1:c.696_699delinsCTCT	XP_011522933.1:p.Ser232=
XM_006721823.2:c.696_699delinsCTCT	XP_006721886.1:p.Ser232=
XM_006721824.4:c.696_699delinsCTCT	XP_006721887.1:p.Ser232=
XM_011524628.3:c.696_699delinsCTCT	XP_011522930.1:p.Ser232=
XM_011524629.3:c.696_699delinsCTCT	XP_011522931.1:p.Ser232=
XM_011524630.3:c.696_699delinsCTCT	XP_011522932.1:p.Ser232=
XM_011524631.3:c.696_699delinsCTCT	XP_011522933.1:p.Ser232=
XM_017024488.2:c.696_699delinsCTCT	XP_016879977.1:p.Ser232=
XM_017024489.1:c.696_699delinsCTCT	XP_016879978.1:p.Ser232=
NM_001193466.2:c.696_699delinsCTCT	NP_001180395.1:p.Ser232=
NM_015443.4:c.696_699delinsCTCT MANE Select	NP_056258.1:p.Ser232=
NM_001193465.2:c.696_699delinsCTCT	NP_001180394.1:p.Ser232=
NM_001379198.1:c.696_699delinsCTCT	NP_001366127.1:p.Ser232=