Canonical Allele Identifier: CA2262110786

Gene: KANSL1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46031658G= , CM000679.2:g.46031658G=	GRCh38
NC_000017.10:g.44109024G= , CM000679.1:g.44109024G=	GRCh37
NC_000017.9:g.41464871G=	NCBI36
NG_032784.1:g.198717C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.3136C= MANE Select	ENSP00000387393.3:p.Pro1046=
ENST00000572904.6:c.3136C=	ENSP00000461484.1:p.Pro1046=
ENST00000574590.6:c.3133C=	ENSP00000461812.2:p.Pro1045=
ENST00000575318.6:c.2944C=	ENSP00000461299.1:p.Pro982=
ENST00000638275.1:c.2944C=	ENSP00000492576.1:p.Pro982=
ENST00000639805.1:n.553C=
ENST00000648792.1:c.3004C=	ENSP00000497628.1:p.Pro1002=
ENST00000262419.10:c.3136C=	ENSP00000262419.6:p.Pro1046=
ENST00000432791.5:c.3133C=	ENSP00000387393.2:p.Pro1045=
ENST00000572218.5:n.7353C=
ENST00000572904.5:c.3136C=	ENSP00000461484.1:p.Pro1046=
ENST00000574590.5:c.3136C=	ENSP00000461812.1:p.Pro1046=
ENST00000574963.1:n.909C=
ENST00000575318.5:c.2944C=	ENSP00000461299.1:p.Pro982=
ENST00000576870.5:n.1108C=
NM_001193465.1:c.3133C=	NP_001180394.1:p.Pro1045=
NM_001193466.1:c.3136C=	NP_001180395.1:p.Pro1046=
NM_015443.3:c.3136C=	NP_056258.1:p.Pro1046=
XM_006721823.1:c.3136C=	XP_006721886.1:p.Pro1046=
XM_006721824.2:c.3136C=	XP_006721887.1:p.Pro1046=
XM_011524628.1:c.3133C=	XP_011522930.1:p.Pro1045=
XM_011524629.1:c.3034C=	XP_011522931.1:p.Pro1012=
XM_011524630.1:c.2947C=	XP_011522932.1:p.Pro983=
XM_011524631.1:c.2944C=	XP_011522933.1:p.Pro982=
XM_011524632.1:c.1906C=	XP_011522934.1:p.Pro636=
XM_006721823.2:c.3136C=	XP_006721886.1:p.Pro1046=
XM_006721824.4:c.3136C=	XP_006721887.1:p.Pro1046=
XM_011524628.3:c.3133C=	XP_011522930.1:p.Pro1045=
XM_011524629.3:c.3034C=	XP_011522931.1:p.Pro1012=
XM_011524630.3:c.2947C=	XP_011522932.1:p.Pro983=
XM_011524631.3:c.2944C=	XP_011522933.1:p.Pro982=
XM_011524632.3:c.1906C=	XP_011522934.1:p.Pro636=
XM_017024488.2:c.2944C=	XP_016879977.1:p.Pro982=
NM_001193466.2:c.3136C=	NP_001180395.1:p.Pro1046=
NM_015443.4:c.3136C= MANE Select	NP_056258.1:p.Pro1046=
NM_001193465.2:c.3133C=	NP_001180394.1:p.Pro1045=
NM_001379198.1:c.3136C=	NP_001366127.1:p.Pro1046=