Canonical Allele Identifier: CA399986749
Gene: KANSL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46032157T>A , CM000679.2:g.46032157T>A GRCh38
NC_000017.10:g.44109523T>A , CM000679.1:g.44109523T>A GRCh37
NC_000017.9:g.41465370T>A NCBI36
NG_032784.1:g.198218A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000432791.7:c.2980A>T MANE Select ENSP00000387393.3:p.Ser994Cys
ENST00000572904.6:c.2980A>T ENSP00000461484.1:p.Ser994Cys
ENST00000574590.6:c.2977A>T ENSP00000461812.2:p.Ser993Cys
ENST00000575318.6:c.2788A>T ENSP00000461299.1:p.Ser930Cys
ENST00000638275.1:c.2788A>T ENSP00000492576.1:p.Ser930Cys
ENST00000639467.1:c.637A>T ENSP00000492741.1:p.Ser213Cys
ENST00000639805.1:n.397A>T
ENST00000648792.1:c.2848A>T ENSP00000497628.1:p.Ser950Cys
ENST00000262419.10:c.2980A>T ENSP00000262419.6:p.Ser994Cys
ENST00000432791.5:c.2977A>T ENSP00000387393.2:p.Ser993Cys
ENST00000572218.5:n.7197A>T
ENST00000572904.5:c.2980A>T ENSP00000461484.1:p.Ser994Cys
ENST00000574590.5:c.2980A>T ENSP00000461812.1:p.Ser994Cys
ENST00000574963.1:n.410A>T
ENST00000575318.5:c.2788A>T ENSP00000461299.1:p.Ser930Cys
ENST00000576870.5:n.952A>T
NM_001193465.1:c.2977A>T NP_001180394.1:p.Ser993Cys
NM_001193466.1:c.2980A>T NP_001180395.1:p.Ser994Cys
NM_015443.3:c.2980A>T NP_056258.1:p.Ser994Cys
XM_006721823.1:c.2980A>T XP_006721886.1:p.Ser994Cys
XM_006721824.2:c.2980A>T XP_006721887.1:p.Ser994Cys
XM_011524628.1:c.2977A>T XP_011522930.1:p.Ser993Cys
XM_011524629.1:c.2878A>T XP_011522931.1:p.Ser960Cys
XM_011524630.1:c.2791A>T XP_011522932.1:p.Ser931Cys
XM_011524631.1:c.2788A>T XP_011522933.1:p.Ser930Cys
XM_011524632.1:c.1750A>T XP_011522934.1:p.Ser584Cys
XM_006721823.2:c.2980A>T XP_006721886.1:p.Ser994Cys
XM_006721824.4:c.2980A>T XP_006721887.1:p.Ser994Cys
XM_011524628.3:c.2977A>T XP_011522930.1:p.Ser993Cys
XM_011524629.3:c.2878A>T XP_011522931.1:p.Ser960Cys
XM_011524630.3:c.2791A>T XP_011522932.1:p.Ser931Cys
XM_011524631.3:c.2788A>T XP_011522933.1:p.Ser930Cys
XM_011524632.3:c.1750A>T XP_011522934.1:p.Ser584Cys
XM_017024488.2:c.2788A>T XP_016879977.1:p.Ser930Cys
NM_001193466.2:c.2980A>T NP_001180395.1:p.Ser994Cys
NM_015443.4:c.2980A>T MANE Select NP_056258.1:p.Ser994Cys
NM_001193465.2:c.2977A>T NP_001180394.1:p.Ser993Cys
NM_001379198.1:c.2980A>T NP_001366127.1:p.Ser994Cys