Canonical Allele Identifier: CA2262110727

Gene: KANSL1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46031534G= , CM000679.2:g.46031534G=	GRCh38
NC_000017.10:g.44108900G= , CM000679.1:g.44108900G=	GRCh37
NC_000017.9:g.41464747G=	NCBI36
NG_032784.1:g.198841C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.3260C= MANE Select	ENSP00000387393.3:p.Pro1087=
ENST00000572904.6:c.3260C=	ENSP00000461484.1:p.Pro1087=
ENST00000574590.6:c.3257C=	ENSP00000461812.2:p.Pro1086=
ENST00000575318.6:c.3068C=	ENSP00000461299.1:p.Pro1023=
ENST00000638275.1:c.3068C=	ENSP00000492576.1:p.Pro1023=
ENST00000648792.1:c.3128C=	ENSP00000497628.1:p.Pro1043=
ENST00000262419.10:c.3260C=	ENSP00000262419.6:p.Pro1087=
ENST00000432791.5:c.3257C=	ENSP00000387393.2:p.Pro1086=
ENST00000572218.5:n.7477C=
ENST00000572904.5:c.3260C=	ENSP00000461484.1:p.Pro1087=
ENST00000574590.5:c.3260C=	ENSP00000461812.1:p.Pro1087=
ENST00000574963.1:n.1033C=
ENST00000575318.5:c.3068C=	ENSP00000461299.1:p.Pro1023=
ENST00000576870.5:n.1232C=
NM_001193465.1:c.3257C=	NP_001180394.1:p.Pro1086=
NM_001193466.1:c.3260C=	NP_001180395.1:p.Pro1087=
NM_015443.3:c.3260C=	NP_056258.1:p.Pro1087=
XM_006721823.1:c.3260C=	XP_006721886.1:p.Pro1087=
XM_006721824.2:c.3260C=	XP_006721887.1:p.Pro1087=
XM_011524628.1:c.3257C=	XP_011522930.1:p.Pro1086=
XM_011524629.1:c.3158C=	XP_011522931.1:p.Pro1053=
XM_011524630.1:c.3071C=	XP_011522932.1:p.Pro1024=
XM_011524631.1:c.3068C=	XP_011522933.1:p.Pro1023=
XM_011524632.1:c.2030C=	XP_011522934.1:p.Pro677=
XM_006721823.2:c.3260C=	XP_006721886.1:p.Pro1087=
XM_006721824.4:c.3260C=	XP_006721887.1:p.Pro1087=
XM_011524628.3:c.3257C=	XP_011522930.1:p.Pro1086=
XM_011524629.3:c.3158C=	XP_011522931.1:p.Pro1053=
XM_011524630.3:c.3071C=	XP_011522932.1:p.Pro1024=
XM_011524631.3:c.3068C=	XP_011522933.1:p.Pro1023=
XM_011524632.3:c.2030C=	XP_011522934.1:p.Pro677=
XM_017024488.2:c.3068C=	XP_016879977.1:p.Pro1023=
NM_001193466.2:c.3260C=	NP_001180395.1:p.Pro1087=
NM_015443.4:c.3260C= MANE Select	NP_056258.1:p.Pro1087=
NM_001193465.2:c.3257C=	NP_001180394.1:p.Pro1086=
NM_001379198.1:c.3260C=	NP_001366127.1:p.Pro1087=