Canonical Allele Identifier: CA2262113784

Gene: KANSL1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46038617G= , CM000679.2:g.46038617G=	GRCh38
NC_000017.10:g.44115983G= , CM000679.1:g.44115983G=	GRCh37
NC_000017.9:g.41471830G=	NCBI36
NG_032784.1:g.191758C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000432791.7:c.2462C= MANE Select	ENSP00000387393.3:p.Pro821=
ENST00000572904.6:c.2462C=	ENSP00000461484.1:p.Pro821=
ENST00000573286.2:n.4145C=
ENST00000574590.6:c.2462C=	ENSP00000461812.2:p.Pro821=
ENST00000575318.6:c.2273C=	ENSP00000461299.1:p.Pro758=
ENST00000576137.2:n.459C=
ENST00000638275.1:c.2273C=	ENSP00000492576.1:p.Pro758=
ENST00000639150.1:c.1196C=	ENSP00000491906.1:p.Pro399=
ENST00000639467.1:c.125C=	ENSP00000492741.1:p.Pro42=
ENST00000639531.1:c.2273C=	ENSP00000491765.1:p.Pro758=
ENST00000640636.1:c.415C=
ENST00000648792.1:c.2462C=	ENSP00000497628.1:p.Pro821=
ENST00000262419.10:c.2462C=	ENSP00000262419.6:p.Pro821=
ENST00000432791.5:c.2462C=	ENSP00000387393.2:p.Pro821=
ENST00000572218.5:n.6679C=
ENST00000572904.5:c.2462C=	ENSP00000461484.1:p.Pro821=
ENST00000573286.1:n.318C=
ENST00000574590.5:c.2462C=	ENSP00000461812.1:p.Pro821=
ENST00000575318.5:c.2273C=	ENSP00000461299.1:p.Pro758=
ENST00000576137.1:n.101C=
ENST00000576870.5:n.434C=
NM_001193465.1:c.2462C=	NP_001180394.1:p.Pro821=
NM_001193466.1:c.2462C=	NP_001180395.1:p.Pro821=
NM_015443.3:c.2462C=	NP_056258.1:p.Pro821=
XM_006721823.1:c.2462C=	XP_006721886.1:p.Pro821=
XM_006721824.2:c.2462C=	XP_006721887.1:p.Pro821=
XM_011524628.1:c.2462C=	XP_011522930.1:p.Pro821=
XM_011524629.1:c.2360C=	XP_011522931.1:p.Pro787=
XM_011524630.1:c.2273C=	XP_011522932.1:p.Pro758=
XM_011524631.1:c.2273C=	XP_011522933.1:p.Pro758=
XM_011524632.1:c.1232C=	XP_011522934.1:p.Pro411=
XM_006721823.2:c.2462C=	XP_006721886.1:p.Pro821=
XM_006721824.4:c.2462C=	XP_006721887.1:p.Pro821=
XM_011524628.3:c.2462C=	XP_011522930.1:p.Pro821=
XM_011524629.3:c.2360C=	XP_011522931.1:p.Pro787=
XM_011524630.3:c.2273C=	XP_011522932.1:p.Pro758=
XM_011524631.3:c.2273C=	XP_011522933.1:p.Pro758=
XM_011524632.3:c.1232C=	XP_011522934.1:p.Pro411=
XM_017024488.2:c.2273C=	XP_016879977.1:p.Pro758=
XM_017024489.1:c.2360C=	XP_016879978.1:p.Pro787=
NM_001193466.2:c.2462C=	NP_001180395.1:p.Pro821=
NM_015443.4:c.2462C= MANE Select	NP_056258.1:p.Pro821=
NM_001193465.2:c.2462C=	NP_001180394.1:p.Pro821=
NM_001379198.1:c.2462C=	NP_001366127.1:p.Pro821=