Canonical Allele Identifier: CA2638372159
Gene: KANSL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46032112del , CM000679.2:g.46032112del GRCh38
NC_000017.10:g.44109478del , CM000679.1:g.44109478del GRCh37
NC_000017.9:g.41465325del NCBI36
NG_032784.1:g.198263del

Transcript Alleles

HGVS Amino-acid Change
ENST00000432791.7:c.3025del MANE Select ENSP00000387393.3:p.Thr1009LeufsTer5
ENST00000572904.6:c.3025del ENSP00000461484.1:p.Thr1009LeufsTer5
ENST00000574590.6:c.3022del ENSP00000461812.2:p.Thr1008LeufsTer5
ENST00000575318.6:c.2833del ENSP00000461299.1:p.Thr945LeufsTer5
ENST00000638275.1:c.2833del ENSP00000492576.1:p.Thr945LeufsTer5
ENST00000639805.1:n.442del
ENST00000648792.1:c.2893del ENSP00000497628.1:p.Thr965LeufsTer5
ENST00000262419.10:c.3025del ENSP00000262419.6:p.Thr1009LeufsTer5
ENST00000432791.5:c.3022del ENSP00000387393.2:p.Thr1008LeufsTer5
ENST00000572218.5:n.7242del
ENST00000572904.5:c.3025del ENSP00000461484.1:p.Thr1009LeufsTer5
ENST00000574590.5:c.3025del ENSP00000461812.1:p.Thr1009LeufsTer5
ENST00000574963.1:n.455del
ENST00000575318.5:c.2833del ENSP00000461299.1:p.Thr945LeufsTer5
ENST00000576870.5:n.997del
NM_001193465.1:c.3022del NP_001180394.1:p.Thr1008LeufsTer5
NM_001193466.1:c.3025del NP_001180395.1:p.Thr1009LeufsTer5
NM_015443.3:c.3025del NP_056258.1:p.Thr1009LeufsTer5
XM_006721823.1:c.3025del XP_006721886.1:p.Thr1009LeufsTer5
XM_006721824.2:c.3025del XP_006721887.1:p.Thr1009LeufsTer5
XM_011524628.1:c.3022del XP_011522930.1:p.Thr1008LeufsTer5
XM_011524629.1:c.2923del XP_011522931.1:p.Thr975LeufsTer5
XM_011524630.1:c.2836del XP_011522932.1:p.Thr946LeufsTer5
XM_011524631.1:c.2833del XP_011522933.1:p.Thr945LeufsTer5
XM_011524632.1:c.1795del XP_011522934.1:p.Thr599LeufsTer5
XM_006721823.2:c.3025del XP_006721886.1:p.Thr1009LeufsTer5
XM_006721824.4:c.3025del XP_006721887.1:p.Thr1009LeufsTer5
XM_011524628.3:c.3022del XP_011522930.1:p.Thr1008LeufsTer5
XM_011524629.3:c.2923del XP_011522931.1:p.Thr975LeufsTer5
XM_011524630.3:c.2836del XP_011522932.1:p.Thr946LeufsTer5
XM_011524631.3:c.2833del XP_011522933.1:p.Thr945LeufsTer5
XM_011524632.3:c.1795del XP_011522934.1:p.Thr599LeufsTer5
XM_017024488.2:c.2833del XP_016879977.1:p.Thr945LeufsTer5
NM_001193466.2:c.3025del NP_001180395.1:p.Thr1009LeufsTer5
NM_015443.4:c.3025del MANE Select NP_056258.1:p.Thr1009LeufsTer5
NM_001193465.2:c.3022del NP_001180394.1:p.Thr1008LeufsTer5
NM_001379198.1:c.3025del NP_001366127.1:p.Thr1009LeufsTer5