Canonical Allele Identifier: CA2262111085

Gene: KANSL1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46032288G= , CM000679.2:g.46032288G=	GRCh38
NC_000017.10:g.44109654G= , CM000679.1:g.44109654G=	GRCh37
NC_000017.9:g.41465501G=	NCBI36
NG_032784.1:g.198087C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.2849C= MANE Select	ENSP00000387393.3:p.Ser950=
ENST00000572904.6:c.2849C=	ENSP00000461484.1:p.Ser950=
ENST00000574590.6:c.2846C=	ENSP00000461812.2:p.Ser949=
ENST00000575318.6:c.2657C=	ENSP00000461299.1:p.Ser886=
ENST00000638275.1:c.2657C=	ENSP00000492576.1:p.Ser886=
ENST00000638291.1:n.677C=
ENST00000638551.1:n.797C=
ENST00000639467.1:c.506C=	ENSP00000492741.1:p.Ser169=
ENST00000639531.1:c.2660C=	ENSP00000491765.1:p.Ser887=
ENST00000639805.1:n.266C=
ENST00000640751.1:n.444C=
ENST00000648792.1:c.2838-121C=	ENSP00000497628.1:n.2838-121C=
ENST00000262419.10:c.2849C=	ENSP00000262419.6:p.Ser950=
ENST00000432791.5:c.2846C=	ENSP00000387393.2:p.Ser949=
ENST00000572218.5:n.7066C=
ENST00000572904.5:c.2849C=	ENSP00000461484.1:p.Ser950=
ENST00000573682.1:n.235C=
ENST00000574590.5:c.2849C=	ENSP00000461812.1:p.Ser950=
ENST00000574963.1:n.279C=
ENST00000575318.5:c.2657C=	ENSP00000461299.1:p.Ser886=
ENST00000576870.5:n.821C=
NM_001193465.1:c.2846C=	NP_001180394.1:p.Ser949=
NM_001193466.1:c.2849C=	NP_001180395.1:p.Ser950=
NM_015443.3:c.2849C=	NP_056258.1:p.Ser950=
XM_006721823.1:c.2849C=	XP_006721886.1:p.Ser950=
XM_006721824.2:c.2849C=	XP_006721887.1:p.Ser950=
XM_011524628.1:c.2846C=	XP_011522930.1:p.Ser949=
XM_011524629.1:c.2747C=	XP_011522931.1:p.Ser916=
XM_011524630.1:c.2660C=	XP_011522932.1:p.Ser887=
XM_011524631.1:c.2657C=	XP_011522933.1:p.Ser886=
XM_011524632.1:c.1619C=	XP_011522934.1:p.Ser540=
XM_006721823.2:c.2849C=	XP_006721886.1:p.Ser950=
XM_006721824.4:c.2849C=	XP_006721887.1:p.Ser950=
XM_011524628.3:c.2846C=	XP_011522930.1:p.Ser949=
XM_011524629.3:c.2747C=	XP_011522931.1:p.Ser916=
XM_011524630.3:c.2660C=	XP_011522932.1:p.Ser887=
XM_011524631.3:c.2657C=	XP_011522933.1:p.Ser886=
XM_011524632.3:c.1619C=	XP_011522934.1:p.Ser540=
XM_017024488.2:c.2657C=	XP_016879977.1:p.Ser886=
NM_001193466.2:c.2849C=	NP_001180395.1:p.Ser950=
NM_015443.4:c.2849C= MANE Select	NP_056258.1:p.Ser950=
NM_001193465.2:c.2846C=	NP_001180394.1:p.Ser949=
NM_001379198.1:c.2849C=	NP_001366127.1:p.Ser950=