Canonical Allele Identifier: CA2262111060
Gene: KANSL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46032239G= , CM000679.2:g.46032239G= GRCh38
NC_000017.10:g.44109605G= , CM000679.1:g.44109605G= GRCh37
NC_000017.9:g.41465452G= NCBI36
NG_032784.1:g.198136C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000432791.7:c.2898C= MANE Select ENSP00000387393.3:p.Thr966=
ENST00000572904.6:c.2898C= ENSP00000461484.1:p.Thr966=
ENST00000574590.6:c.2895C= ENSP00000461812.2:p.Thr965=
ENST00000575318.6:c.2706C= ENSP00000461299.1:p.Thr902=
ENST00000638275.1:c.2706C= ENSP00000492576.1:p.Thr902=
ENST00000638291.1:n.726C=
ENST00000638551.1:n.846C=
ENST00000639467.1:c.555C= ENSP00000492741.1:p.Thr185=
ENST00000639805.1:n.315C=
ENST00000648792.1:c.2838-72C= ENSP00000497628.1:n.2838-72C=
ENST00000262419.10:c.2898C= ENSP00000262419.6:p.Thr966=
ENST00000432791.5:c.2895C= ENSP00000387393.2:p.Thr965=
ENST00000572218.5:n.7115C=
ENST00000572904.5:c.2898C= ENSP00000461484.1:p.Thr966=
ENST00000573682.1:n.284C=
ENST00000574590.5:c.2898C= ENSP00000461812.1:p.Thr966=
ENST00000574963.1:n.328C=
ENST00000575318.5:c.2706C= ENSP00000461299.1:p.Thr902=
ENST00000576870.5:n.870C=
NM_001193465.1:c.2895C= NP_001180394.1:p.Thr965=
NM_001193466.1:c.2898C= NP_001180395.1:p.Thr966=
NM_015443.3:c.2898C= NP_056258.1:p.Thr966=
XM_006721823.1:c.2898C= XP_006721886.1:p.Thr966=
XM_006721824.2:c.2898C= XP_006721887.1:p.Thr966=
XM_011524628.1:c.2895C= XP_011522930.1:p.Thr965=
XM_011524629.1:c.2796C= XP_011522931.1:p.Thr932=
XM_011524630.1:c.2709C= XP_011522932.1:p.Thr903=
XM_011524631.1:c.2706C= XP_011522933.1:p.Thr902=
XM_011524632.1:c.1668C= XP_011522934.1:p.Thr556=
XM_006721823.2:c.2898C= XP_006721886.1:p.Thr966=
XM_006721824.4:c.2898C= XP_006721887.1:p.Thr966=
XM_011524628.3:c.2895C= XP_011522930.1:p.Thr965=
XM_011524629.3:c.2796C= XP_011522931.1:p.Thr932=
XM_011524630.3:c.2709C= XP_011522932.1:p.Thr903=
XM_011524631.3:c.2706C= XP_011522933.1:p.Thr902=
XM_011524632.3:c.1668C= XP_011522934.1:p.Thr556=
XM_017024488.2:c.2706C= XP_016879977.1:p.Thr902=
NM_001193466.2:c.2898C= NP_001180395.1:p.Thr966=
NM_015443.4:c.2898C= MANE Select NP_056258.1:p.Thr966=
NM_001193465.2:c.2895C= NP_001180394.1:p.Thr965=
NM_001379198.1:c.2898C= NP_001366127.1:p.Thr966=