Canonical Allele Identifier: CA2262127862

Gene: KANSL1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46067646A= , CM000679.2:g.46067646A=	GRCh38
NC_000017.9:g.41500834A=	NCBI36
NG_032784.1:g.162729T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.1555T= MANE Select	ENSP00000387393.3:p.Leu519=
ENST00000571698.2:c.1555T=	ENSP00000459330.2:p.Leu519=
ENST00000572904.6:c.1555T=	ENSP00000461484.1:p.Leu519=
ENST00000574590.6:c.1555T=	ENSP00000461812.2:p.Leu519=
ENST00000575318.6:c.1555T=	ENSP00000461299.1:p.Leu519=
ENST00000577114.2:n.281T=
ENST00000638275.1:c.1555T=	ENSP00000492576.1:p.Leu519=
ENST00000639150.1:c.289T=	ENSP00000491906.1:p.Leu97=
ENST00000639375.1:n.1793T=
ENST00000639531.1:c.1555T=	ENSP00000491765.1:p.Leu519=
ENST00000639853.1:c.726T=
ENST00000648792.1:c.1555T=	ENSP00000497628.1:p.Leu519=
ENST00000262419.10:c.1555T=	ENSP00000262419.6:p.Leu519=
ENST00000432791.5:c.1555T=	ENSP00000387393.2:p.Leu519=
ENST00000572904.5:c.1555T=	ENSP00000461484.1:p.Leu519=
ENST00000574590.5:c.1555T=	ENSP00000461812.1:p.Leu519=
ENST00000575318.5:c.1555T=	ENSP00000461299.1:p.Leu519=
ENST00000577114.1:n.352T=
NM_001193465.1:c.1555T=	NP_001180394.1:p.Leu519=
NM_001193466.1:c.1555T=	NP_001180395.1:p.Leu519=
NM_015443.3:c.1555T=	NP_056258.1:p.Leu519=
XM_006721823.1:c.1555T=	XP_006721886.1:p.Leu519=
XM_006721824.2:c.1555T=	XP_006721887.1:p.Leu519=
XM_011524628.1:c.1555T=	XP_011522930.1:p.Leu519=
XM_011524629.1:c.1453T=	XP_011522931.1:p.Leu485=
XM_011524630.1:c.1555T=	XP_011522932.1:p.Leu519=
XM_011524631.1:c.1555T=	XP_011522933.1:p.Leu519=
XM_011524632.1:c.325T=	XP_011522934.1:p.Leu109=
XM_006721823.2:c.1555T=	XP_006721886.1:p.Leu519=
XM_006721824.4:c.1555T=	XP_006721887.1:p.Leu519=
XM_011524628.3:c.1555T=	XP_011522930.1:p.Leu519=
XM_011524629.3:c.1453T=	XP_011522931.1:p.Leu485=
XM_011524630.3:c.1555T=	XP_011522932.1:p.Leu519=
XM_011524631.3:c.1555T=	XP_011522933.1:p.Leu519=
XM_011524632.3:c.325T=	XP_011522934.1:p.Leu109=
XM_017024488.2:c.1555T=	XP_016879977.1:p.Leu519=
XM_017024489.1:c.1453T=	XP_016879978.1:p.Leu485=
NM_001193466.2:c.1555T=	NP_001180395.1:p.Leu519=
NM_015443.4:c.1555T= MANE Select	NP_056258.1:p.Leu519=
NM_001193465.2:c.1555T=	NP_001180394.1:p.Leu519=
NM_001379198.1:c.1555T=	NP_001366127.1:p.Leu519=