Canonical Allele Identifier: CA2262111087

Gene: KANSL1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46032293G= , CM000679.2:g.46032293G=	GRCh38
NC_000017.10:g.44109659G= , CM000679.1:g.44109659G=	GRCh37
NC_000017.9:g.41465506G=	NCBI36
NG_032784.1:g.198082C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.2844C= MANE Select	ENSP00000387393.3:p.Tyr948=
ENST00000572904.6:c.2844C=	ENSP00000461484.1:p.Tyr948=
ENST00000574590.6:c.2841C=	ENSP00000461812.2:p.Tyr947=
ENST00000575318.6:c.2652C=	ENSP00000461299.1:p.Tyr884=
ENST00000638275.1:c.2652C=	ENSP00000492576.1:p.Tyr884=
ENST00000638291.1:n.672C=
ENST00000638551.1:n.792C=
ENST00000639467.1:c.501C=	ENSP00000492741.1:p.Tyr167=
ENST00000639531.1:c.2655C=	ENSP00000491765.1:p.Tyr885=
ENST00000639805.1:n.261C=
ENST00000640751.1:n.439C=
ENST00000648792.1:c.2838-126C=	ENSP00000497628.1:n.2838-126C=
ENST00000262419.10:c.2844C=	ENSP00000262419.6:p.Tyr948=
ENST00000432791.5:c.2841C=	ENSP00000387393.2:p.Tyr947=
ENST00000572218.5:n.7061C=
ENST00000572904.5:c.2844C=	ENSP00000461484.1:p.Tyr948=
ENST00000573682.1:n.230C=
ENST00000574590.5:c.2844C=	ENSP00000461812.1:p.Tyr948=
ENST00000574963.1:n.274C=
ENST00000575318.5:c.2652C=	ENSP00000461299.1:p.Tyr884=
ENST00000576870.5:n.816C=
NM_001193465.1:c.2841C=	NP_001180394.1:p.Tyr947=
NM_001193466.1:c.2844C=	NP_001180395.1:p.Tyr948=
NM_015443.3:c.2844C=	NP_056258.1:p.Tyr948=
XM_006721823.1:c.2844C=	XP_006721886.1:p.Tyr948=
XM_006721824.2:c.2844C=	XP_006721887.1:p.Tyr948=
XM_011524628.1:c.2841C=	XP_011522930.1:p.Tyr947=
XM_011524629.1:c.2742C=	XP_011522931.1:p.Tyr914=
XM_011524630.1:c.2655C=	XP_011522932.1:p.Tyr885=
XM_011524631.1:c.2652C=	XP_011522933.1:p.Tyr884=
XM_011524632.1:c.1614C=	XP_011522934.1:p.Tyr538=
XM_006721823.2:c.2844C=	XP_006721886.1:p.Tyr948=
XM_006721824.4:c.2844C=	XP_006721887.1:p.Tyr948=
XM_011524628.3:c.2841C=	XP_011522930.1:p.Tyr947=
XM_011524629.3:c.2742C=	XP_011522931.1:p.Tyr914=
XM_011524630.3:c.2655C=	XP_011522932.1:p.Tyr885=
XM_011524631.3:c.2652C=	XP_011522933.1:p.Tyr884=
XM_011524632.3:c.1614C=	XP_011522934.1:p.Tyr538=
XM_017024488.2:c.2652C=	XP_016879977.1:p.Tyr884=
NM_001193466.2:c.2844C=	NP_001180395.1:p.Tyr948=
NM_015443.4:c.2844C= MANE Select	NP_056258.1:p.Tyr948=
NM_001193465.2:c.2841C=	NP_001180394.1:p.Tyr947=
NM_001379198.1:c.2844C=	NP_001366127.1:p.Tyr948=