Canonical Allele Identifier: CA2262110791

Gene: KANSL1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46031665C= , CM000679.2:g.46031665C=	GRCh38
NC_000017.10:g.44109031C= , CM000679.1:g.44109031C=	GRCh37
NC_000017.9:g.41464878C=	NCBI36
NG_032784.1:g.198710G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.3129G= MANE Select	ENSP00000387393.3:p.Ala1043=
ENST00000572904.6:c.3129G=	ENSP00000461484.1:p.Ala1043=
ENST00000574590.6:c.3126G=	ENSP00000461812.2:p.Ala1042=
ENST00000575318.6:c.2937G=	ENSP00000461299.1:p.Ala979=
ENST00000638275.1:c.2937G=	ENSP00000492576.1:p.Ala979=
ENST00000639805.1:n.546G=
ENST00000648792.1:c.2997G=	ENSP00000497628.1:p.Ala999=
ENST00000262419.10:c.3129G=	ENSP00000262419.6:p.Ala1043=
ENST00000432791.5:c.3126G=	ENSP00000387393.2:p.Ala1042=
ENST00000572218.5:n.7346G=
ENST00000572904.5:c.3129G=	ENSP00000461484.1:p.Ala1043=
ENST00000574590.5:c.3129G=	ENSP00000461812.1:p.Ala1043=
ENST00000574963.1:n.902G=
ENST00000575318.5:c.2937G=	ENSP00000461299.1:p.Ala979=
ENST00000576870.5:n.1101G=
NM_001193465.1:c.3126G=	NP_001180394.1:p.Ala1042=
NM_001193466.1:c.3129G=	NP_001180395.1:p.Ala1043=
NM_015443.3:c.3129G=	NP_056258.1:p.Ala1043=
XM_006721823.1:c.3129G=	XP_006721886.1:p.Ala1043=
XM_006721824.2:c.3129G=	XP_006721887.1:p.Ala1043=
XM_011524628.1:c.3126G=	XP_011522930.1:p.Ala1042=
XM_011524629.1:c.3027G=	XP_011522931.1:p.Ala1009=
XM_011524630.1:c.2940G=	XP_011522932.1:p.Ala980=
XM_011524631.1:c.2937G=	XP_011522933.1:p.Ala979=
XM_011524632.1:c.1899G=	XP_011522934.1:p.Ala633=
XM_006721823.2:c.3129G=	XP_006721886.1:p.Ala1043=
XM_006721824.4:c.3129G=	XP_006721887.1:p.Ala1043=
XM_011524628.3:c.3126G=	XP_011522930.1:p.Ala1042=
XM_011524629.3:c.3027G=	XP_011522931.1:p.Ala1009=
XM_011524630.3:c.2940G=	XP_011522932.1:p.Ala980=
XM_011524631.3:c.2937G=	XP_011522933.1:p.Ala979=
XM_011524632.3:c.1899G=	XP_011522934.1:p.Ala633=
XM_017024488.2:c.2937G=	XP_016879977.1:p.Ala979=
NM_001193466.2:c.3129G=	NP_001180395.1:p.Ala1043=
NM_015443.4:c.3129G= MANE Select	NP_056258.1:p.Ala1043=
NM_001193465.2:c.3126G=	NP_001180394.1:p.Ala1042=
NM_001379198.1:c.3129G=	NP_001366127.1:p.Ala1043=