Canonical Allele Identifier: CA399986774
Gene: KANSL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46032160T>G , CM000679.2:g.46032160T>G GRCh38
NC_000017.10:g.44109526T>G , CM000679.1:g.44109526T>G GRCh37
NC_000017.9:g.41465373T>G NCBI36
NG_032784.1:g.198215A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000432791.7:c.2977A>C MANE Select ENSP00000387393.3:p.Ile993Leu
ENST00000572904.6:c.2977A>C ENSP00000461484.1:p.Ile993Leu
ENST00000574590.6:c.2974A>C ENSP00000461812.2:p.Ile992Leu
ENST00000575318.6:c.2785A>C ENSP00000461299.1:p.Ile929Leu
ENST00000638275.1:c.2785A>C ENSP00000492576.1:p.Ile929Leu
ENST00000639467.1:c.634A>C ENSP00000492741.1:p.Ile212Leu
ENST00000639805.1:n.394A>C
ENST00000648792.1:c.2845A>C ENSP00000497628.1:p.Ile949Leu
ENST00000262419.10:c.2977A>C ENSP00000262419.6:p.Ile993Leu
ENST00000432791.5:c.2974A>C ENSP00000387393.2:p.Ile992Leu
ENST00000572218.5:n.7194A>C
ENST00000572904.5:c.2977A>C ENSP00000461484.1:p.Ile993Leu
ENST00000574590.5:c.2977A>C ENSP00000461812.1:p.Ile993Leu
ENST00000574963.1:n.407A>C
ENST00000575318.5:c.2785A>C ENSP00000461299.1:p.Ile929Leu
ENST00000576870.5:n.949A>C
NM_001193465.1:c.2974A>C NP_001180394.1:p.Ile992Leu
NM_001193466.1:c.2977A>C NP_001180395.1:p.Ile993Leu
NM_015443.3:c.2977A>C NP_056258.1:p.Ile993Leu
XM_006721823.1:c.2977A>C XP_006721886.1:p.Ile993Leu
XM_006721824.2:c.2977A>C XP_006721887.1:p.Ile993Leu
XM_011524628.1:c.2974A>C XP_011522930.1:p.Ile992Leu
XM_011524629.1:c.2875A>C XP_011522931.1:p.Ile959Leu
XM_011524630.1:c.2788A>C XP_011522932.1:p.Ile930Leu
XM_011524631.1:c.2785A>C XP_011522933.1:p.Ile929Leu
XM_011524632.1:c.1747A>C XP_011522934.1:p.Ile583Leu
XM_006721823.2:c.2977A>C XP_006721886.1:p.Ile993Leu
XM_006721824.4:c.2977A>C XP_006721887.1:p.Ile993Leu
XM_011524628.3:c.2974A>C XP_011522930.1:p.Ile992Leu
XM_011524629.3:c.2875A>C XP_011522931.1:p.Ile959Leu
XM_011524630.3:c.2788A>C XP_011522932.1:p.Ile930Leu
XM_011524631.3:c.2785A>C XP_011522933.1:p.Ile929Leu
XM_011524632.3:c.1747A>C XP_011522934.1:p.Ile583Leu
XM_017024488.2:c.2785A>C XP_016879977.1:p.Ile929Leu
NM_001193466.2:c.2977A>C NP_001180395.1:p.Ile993Leu
NM_015443.4:c.2977A>C MANE Select NP_056258.1:p.Ile993Leu
NM_001193465.2:c.2974A>C NP_001180394.1:p.Ile992Leu
NM_001379198.1:c.2977A>C NP_001366127.1:p.Ile993Leu