Canonical Allele Identifier: CA2262111018
Gene: KANSL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46032133G= , CM000679.2:g.46032133G= GRCh38
NC_000017.10:g.44109499G= , CM000679.1:g.44109499G= GRCh37
NC_000017.9:g.41465346G= NCBI36
NG_032784.1:g.198242C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000432791.7:c.3004C= MANE Select ENSP00000387393.3:p.Leu1002=
ENST00000572904.6:c.3004C= ENSP00000461484.1:p.Leu1002=
ENST00000574590.6:c.3001C= ENSP00000461812.2:p.Leu1001=
ENST00000575318.6:c.2812C= ENSP00000461299.1:p.Leu938=
ENST00000638275.1:c.2812C= ENSP00000492576.1:p.Leu938=
ENST00000639467.1:c.661C= ENSP00000492741.1:p.Leu221=
ENST00000639805.1:n.421C=
ENST00000648792.1:c.2872C= ENSP00000497628.1:p.Leu958=
ENST00000262419.10:c.3004C= ENSP00000262419.6:p.Leu1002=
ENST00000432791.5:c.3001C= ENSP00000387393.2:p.Leu1001=
ENST00000572218.5:n.7221C=
ENST00000572904.5:c.3004C= ENSP00000461484.1:p.Leu1002=
ENST00000574590.5:c.3004C= ENSP00000461812.1:p.Leu1002=
ENST00000574963.1:n.434C=
ENST00000575318.5:c.2812C= ENSP00000461299.1:p.Leu938=
ENST00000576870.5:n.976C=
NM_001193465.1:c.3001C= NP_001180394.1:p.Leu1001=
NM_001193466.1:c.3004C= NP_001180395.1:p.Leu1002=
NM_015443.3:c.3004C= NP_056258.1:p.Leu1002=
XM_006721823.1:c.3004C= XP_006721886.1:p.Leu1002=
XM_006721824.2:c.3004C= XP_006721887.1:p.Leu1002=
XM_011524628.1:c.3001C= XP_011522930.1:p.Leu1001=
XM_011524629.1:c.2902C= XP_011522931.1:p.Leu968=
XM_011524630.1:c.2815C= XP_011522932.1:p.Leu939=
XM_011524631.1:c.2812C= XP_011522933.1:p.Leu938=
XM_011524632.1:c.1774C= XP_011522934.1:p.Leu592=
XM_006721823.2:c.3004C= XP_006721886.1:p.Leu1002=
XM_006721824.4:c.3004C= XP_006721887.1:p.Leu1002=
XM_011524628.3:c.3001C= XP_011522930.1:p.Leu1001=
XM_011524629.3:c.2902C= XP_011522931.1:p.Leu968=
XM_011524630.3:c.2815C= XP_011522932.1:p.Leu939=
XM_011524631.3:c.2812C= XP_011522933.1:p.Leu938=
XM_011524632.3:c.1774C= XP_011522934.1:p.Leu592=
XM_017024488.2:c.2812C= XP_016879977.1:p.Leu938=
NM_001193466.2:c.3004C= NP_001180395.1:p.Leu1002=
NM_015443.4:c.3004C= MANE Select NP_056258.1:p.Leu1002=
NM_001193465.2:c.3001C= NP_001180394.1:p.Leu1001=
NM_001379198.1:c.3004C= NP_001366127.1:p.Leu1002=