Canonical Allele Identifier: CA2262110666
Gene: KANSL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46031420T= , CM000679.2:g.46031420T= GRCh38
NC_000017.10:g.44108786T= , CM000679.1:g.44108786T= GRCh37
NC_000017.9:g.41464633T= NCBI36
NG_032784.1:g.198955A=

Transcript Alleles

HGVS Amino-acid change
ENST00000432791.7:c.*56A= MANE Select ENSP00000387393.3:n.*56A=
ENST00000572904.6:c.*56A= ENSP00000461484.1:n.*56A=
ENST00000574590.6:c.*56A= ENSP00000461812.2:n.*56A=
ENST00000575318.6:c.*56A= ENSP00000461299.1:n.*56A=
ENST00000638275.1:c.*56A= ENSP00000492576.1:n.*56A=
ENST00000648792.1:c.*56A= ENSP00000497628.1:n.*56A=
ENST00000262419.10:c.*56A= ENSP00000262419.6:n.*56A=
ENST00000432791.5:c.*56A= ENSP00000387393.2:n.*56A=
ENST00000572218.5:n.7591A=
ENST00000572904.5:c.*56A= ENSP00000461484.1:n.*56A=
ENST00000574590.5:c.*56A= ENSP00000461812.1:n.*56A=
ENST00000574963.1:n.1147A=
ENST00000575318.5:c.*56A= ENSP00000461299.1:n.*56A=
ENST00000576870.5:n.1346A=
NM_001193465.1:c.*56A= NP_001180394.1:n.*56A=
NM_001193466.1:c.*56A= NP_001180395.1:n.*56A=
NM_015443.3:c.*56A= NP_056258.1:n.*56A=
XM_006721823.1:c.*56A= XP_006721886.1:n.*56A=
XM_006721824.2:c.*56A= XP_006721887.1:n.*56A=
XM_011524628.1:c.*56A= XP_011522930.1:n.*56A=
XM_011524629.1:c.*56A= XP_011522931.1:n.*56A=
XM_011524630.1:c.*56A= XP_011522932.1:n.*56A=
XM_011524631.1:c.*56A= XP_011522933.1:n.*56A=
XM_011524632.1:c.*56A= XP_011522934.1:n.*56A=
XM_006721823.2:c.*56A= XP_006721886.1:n.*56A=
XM_006721824.4:c.*56A= XP_006721887.1:n.*56A=
XM_011524628.3:c.*56A= XP_011522930.1:n.*56A=
XM_011524629.3:c.*56A= XP_011522931.1:n.*56A=
XM_011524630.3:c.*56A= XP_011522932.1:n.*56A=
XM_011524631.3:c.*56A= XP_011522933.1:n.*56A=
XM_011524632.3:c.*56A= XP_011522934.1:n.*56A=
XM_017024488.2:c.*56A= XP_016879977.1:n.*56A=
NM_001193466.2:c.*56A= NP_001180395.1:n.*56A=
NM_015443.4:c.*56A= MANE Select NP_056258.1:n.*56A=
NM_001193465.2:c.*56A= NP_001180394.1:n.*56A=
NM_001379198.1:c.*56A= NP_001366127.1:n.*56A=