Canonical Allele Identifier: CA2262111074

Gene: KANSL1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46032265G= , CM000679.2:g.46032265G=	GRCh38
NC_000017.10:g.44109631G= , CM000679.1:g.44109631G=	GRCh37
NC_000017.9:g.41465478G=	NCBI36
NG_032784.1:g.198110C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.2872C= MANE Select	ENSP00000387393.3:p.Gln958=
ENST00000572904.6:c.2872C=	ENSP00000461484.1:p.Gln958=
ENST00000574590.6:c.2869C=	ENSP00000461812.2:p.Gln957=
ENST00000575318.6:c.2680C=	ENSP00000461299.1:p.Gln894=
ENST00000638275.1:c.2680C=	ENSP00000492576.1:p.Gln894=
ENST00000638291.1:n.700C=
ENST00000638551.1:n.820C=
ENST00000639467.1:c.529C=	ENSP00000492741.1:p.Gln177=
ENST00000639531.1:c.2683C=	ENSP00000491765.1:p.Gln895=
ENST00000639805.1:n.289C=
ENST00000648792.1:c.2838-98C=	ENSP00000497628.1:n.2838-98C=
ENST00000262419.10:c.2872C=	ENSP00000262419.6:p.Gln958=
ENST00000432791.5:c.2869C=	ENSP00000387393.2:p.Gln957=
ENST00000572218.5:n.7089C=
ENST00000572904.5:c.2872C=	ENSP00000461484.1:p.Gln958=
ENST00000573682.1:n.258C=
ENST00000574590.5:c.2872C=	ENSP00000461812.1:p.Gln958=
ENST00000574963.1:n.302C=
ENST00000575318.5:c.2680C=	ENSP00000461299.1:p.Gln894=
ENST00000576870.5:n.844C=
NM_001193465.1:c.2869C=	NP_001180394.1:p.Gln957=
NM_001193466.1:c.2872C=	NP_001180395.1:p.Gln958=
NM_015443.3:c.2872C=	NP_056258.1:p.Gln958=
XM_006721823.1:c.2872C=	XP_006721886.1:p.Gln958=
XM_006721824.2:c.2872C=	XP_006721887.1:p.Gln958=
XM_011524628.1:c.2869C=	XP_011522930.1:p.Gln957=
XM_011524629.1:c.2770C=	XP_011522931.1:p.Gln924=
XM_011524630.1:c.2683C=	XP_011522932.1:p.Gln895=
XM_011524631.1:c.2680C=	XP_011522933.1:p.Gln894=
XM_011524632.1:c.1642C=	XP_011522934.1:p.Gln548=
XM_006721823.2:c.2872C=	XP_006721886.1:p.Gln958=
XM_006721824.4:c.2872C=	XP_006721887.1:p.Gln958=
XM_011524628.3:c.2869C=	XP_011522930.1:p.Gln957=
XM_011524629.3:c.2770C=	XP_011522931.1:p.Gln924=
XM_011524630.3:c.2683C=	XP_011522932.1:p.Gln895=
XM_011524631.3:c.2680C=	XP_011522933.1:p.Gln894=
XM_011524632.3:c.1642C=	XP_011522934.1:p.Gln548=
XM_017024488.2:c.2680C=	XP_016879977.1:p.Gln894=
NM_001193466.2:c.2872C=	NP_001180395.1:p.Gln958=
NM_015443.4:c.2872C= MANE Select	NP_056258.1:p.Gln958=
NM_001193465.2:c.2869C=	NP_001180394.1:p.Gln957=
NM_001379198.1:c.2872C=	NP_001366127.1:p.Gln958=