Canonical Allele Identifier: CA399986713
Gene: KANSL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46032151C>T , CM000679.2:g.46032151C>T GRCh38
NC_000017.10:g.44109517C>T , CM000679.1:g.44109517C>T GRCh37
NC_000017.9:g.41465364C>T NCBI36
NG_032784.1:g.198224G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000432791.7:c.2986G>A MANE Select ENSP00000387393.3:p.Glu996Lys
ENST00000572904.6:c.2986G>A ENSP00000461484.1:p.Glu996Lys
ENST00000574590.6:c.2983G>A ENSP00000461812.2:p.Glu995Lys
ENST00000575318.6:c.2794G>A ENSP00000461299.1:p.Glu932Lys
ENST00000638275.1:c.2794G>A ENSP00000492576.1:p.Glu932Lys
ENST00000639467.1:c.643G>A ENSP00000492741.1:p.Glu215Lys
ENST00000639805.1:n.403G>A
ENST00000648792.1:c.2854G>A ENSP00000497628.1:p.Glu952Lys
ENST00000262419.10:c.2986G>A ENSP00000262419.6:p.Glu996Lys
ENST00000432791.5:c.2983G>A ENSP00000387393.2:p.Glu995Lys
ENST00000572218.5:n.7203G>A
ENST00000572904.5:c.2986G>A ENSP00000461484.1:p.Glu996Lys
ENST00000574590.5:c.2986G>A ENSP00000461812.1:p.Glu996Lys
ENST00000574963.1:n.416G>A
ENST00000575318.5:c.2794G>A ENSP00000461299.1:p.Glu932Lys
ENST00000576870.5:n.958G>A
NM_001193465.1:c.2983G>A NP_001180394.1:p.Glu995Lys
NM_001193466.1:c.2986G>A NP_001180395.1:p.Glu996Lys
NM_015443.3:c.2986G>A NP_056258.1:p.Glu996Lys
XM_006721823.1:c.2986G>A XP_006721886.1:p.Glu996Lys
XM_006721824.2:c.2986G>A XP_006721887.1:p.Glu996Lys
XM_011524628.1:c.2983G>A XP_011522930.1:p.Glu995Lys
XM_011524629.1:c.2884G>A XP_011522931.1:p.Glu962Lys
XM_011524630.1:c.2797G>A XP_011522932.1:p.Glu933Lys
XM_011524631.1:c.2794G>A XP_011522933.1:p.Glu932Lys
XM_011524632.1:c.1756G>A XP_011522934.1:p.Glu586Lys
XM_006721823.2:c.2986G>A XP_006721886.1:p.Glu996Lys
XM_006721824.4:c.2986G>A XP_006721887.1:p.Glu996Lys
XM_011524628.3:c.2983G>A XP_011522930.1:p.Glu995Lys
XM_011524629.3:c.2884G>A XP_011522931.1:p.Glu962Lys
XM_011524630.3:c.2797G>A XP_011522932.1:p.Glu933Lys
XM_011524631.3:c.2794G>A XP_011522933.1:p.Glu932Lys
XM_011524632.3:c.1756G>A XP_011522934.1:p.Glu586Lys
XM_017024488.2:c.2794G>A XP_016879977.1:p.Glu932Lys
NM_001193466.2:c.2986G>A NP_001180395.1:p.Glu996Lys
NM_015443.4:c.2986G>A MANE Select NP_056258.1:p.Glu996Lys
NM_001193465.2:c.2983G>A NP_001180394.1:p.Glu995Lys
NM_001379198.1:c.2986G>A NP_001366127.1:p.Glu996Lys