Canonical Allele Identifier: CA8618423
Gene: KANSL1 HGNC NCBI

Linked Data

dbSNP Id: rs768555471

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46032241T>G , CM000679.2:g.46032241T>G GRCh38
NC_000017.10:g.44109607T>G , CM000679.1:g.44109607T>G GRCh37
NC_000017.9:g.41465454T>G NCBI36
NG_032784.1:g.198134A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000432791.7:c.2896A>C MANE Select ENSP00000387393.3:p.Thr966Pro
ENST00000572904.6:c.2896A>C ENSP00000461484.1:p.Thr966Pro
ENST00000574590.6:c.2893A>C ENSP00000461812.2:p.Thr965Pro
ENST00000575318.6:c.2704A>C ENSP00000461299.1:p.Thr902Pro
ENST00000638275.1:c.2704A>C ENSP00000492576.1:p.Thr902Pro
ENST00000638291.1:n.724A>C
ENST00000638551.1:n.844A>C
ENST00000639467.1:c.553A>C ENSP00000492741.1:p.Thr185Pro
ENST00000639805.1:n.313A>C
ENST00000648792.1:c.2838-74A>C ENSP00000497628.1:n.2838-74A>C
ENST00000262419.10:c.2896A>C ENSP00000262419.6:p.Thr966Pro
ENST00000432791.5:c.2893A>C ENSP00000387393.2:p.Thr965Pro
ENST00000572218.5:n.7113A>C
ENST00000572904.5:c.2896A>C ENSP00000461484.1:p.Thr966Pro
ENST00000573682.1:n.282A>C
ENST00000574590.5:c.2896A>C ENSP00000461812.1:p.Thr966Pro
ENST00000574963.1:n.326A>C
ENST00000575318.5:c.2704A>C ENSP00000461299.1:p.Thr902Pro
ENST00000576870.5:n.868A>C
NM_001193465.1:c.2893A>C NP_001180394.1:p.Thr965Pro
NM_001193466.1:c.2896A>C NP_001180395.1:p.Thr966Pro
NM_015443.3:c.2896A>C NP_056258.1:p.Thr966Pro
XM_006721823.1:c.2896A>C XP_006721886.1:p.Thr966Pro
XM_006721824.2:c.2896A>C XP_006721887.1:p.Thr966Pro
XM_011524628.1:c.2893A>C XP_011522930.1:p.Thr965Pro
XM_011524629.1:c.2794A>C XP_011522931.1:p.Thr932Pro
XM_011524630.1:c.2707A>C XP_011522932.1:p.Thr903Pro
XM_011524631.1:c.2704A>C XP_011522933.1:p.Thr902Pro
XM_011524632.1:c.1666A>C XP_011522934.1:p.Thr556Pro
XM_006721823.2:c.2896A>C XP_006721886.1:p.Thr966Pro
XM_006721824.4:c.2896A>C XP_006721887.1:p.Thr966Pro
XM_011524628.3:c.2893A>C XP_011522930.1:p.Thr965Pro
XM_011524629.3:c.2794A>C XP_011522931.1:p.Thr932Pro
XM_011524630.3:c.2707A>C XP_011522932.1:p.Thr903Pro
XM_011524631.3:c.2704A>C XP_011522933.1:p.Thr902Pro
XM_011524632.3:c.1666A>C XP_011522934.1:p.Thr556Pro
XM_017024488.2:c.2704A>C XP_016879977.1:p.Thr902Pro
NM_001193466.2:c.2896A>C NP_001180395.1:p.Thr966Pro
NM_015443.4:c.2896A>C MANE Select NP_056258.1:p.Thr966Pro
NM_001193465.2:c.2893A>C NP_001180394.1:p.Thr965Pro
NM_001379198.1:c.2896A>C NP_001366127.1:p.Thr966Pro