Canonical Allele Identifier: CA2262110731
Gene: KANSL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46031540A= , CM000679.2:g.46031540A= GRCh38
NC_000017.10:g.44108906A= , CM000679.1:g.44108906A= GRCh37
NC_000017.9:g.41464753A= NCBI36
NG_032784.1:g.198835T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000432791.7:c.3254T= MANE Select ENSP00000387393.3:p.Ile1085=
ENST00000572904.6:c.3254T= ENSP00000461484.1:p.Ile1085=
ENST00000574590.6:c.3251T= ENSP00000461812.2:p.Ile1084=
ENST00000575318.6:c.3062T= ENSP00000461299.1:p.Ile1021=
ENST00000638275.1:c.3062T= ENSP00000492576.1:p.Ile1021=
ENST00000648792.1:c.3122T= ENSP00000497628.1:p.Ile1041=
ENST00000262419.10:c.3254T= ENSP00000262419.6:p.Ile1085=
ENST00000432791.5:c.3251T= ENSP00000387393.2:p.Ile1084=
ENST00000572218.5:n.7471T=
ENST00000572904.5:c.3254T= ENSP00000461484.1:p.Ile1085=
ENST00000574590.5:c.3254T= ENSP00000461812.1:p.Ile1085=
ENST00000574963.1:n.1027T=
ENST00000575318.5:c.3062T= ENSP00000461299.1:p.Ile1021=
ENST00000576870.5:n.1226T=
NM_001193465.1:c.3251T= NP_001180394.1:p.Ile1084=
NM_001193466.1:c.3254T= NP_001180395.1:p.Ile1085=
NM_015443.3:c.3254T= NP_056258.1:p.Ile1085=
XM_006721823.1:c.3254T= XP_006721886.1:p.Ile1085=
XM_006721824.2:c.3254T= XP_006721887.1:p.Ile1085=
XM_011524628.1:c.3251T= XP_011522930.1:p.Ile1084=
XM_011524629.1:c.3152T= XP_011522931.1:p.Ile1051=
XM_011524630.1:c.3065T= XP_011522932.1:p.Ile1022=
XM_011524631.1:c.3062T= XP_011522933.1:p.Ile1021=
XM_011524632.1:c.2024T= XP_011522934.1:p.Ile675=
XM_006721823.2:c.3254T= XP_006721886.1:p.Ile1085=
XM_006721824.4:c.3254T= XP_006721887.1:p.Ile1085=
XM_011524628.3:c.3251T= XP_011522930.1:p.Ile1084=
XM_011524629.3:c.3152T= XP_011522931.1:p.Ile1051=
XM_011524630.3:c.3065T= XP_011522932.1:p.Ile1022=
XM_011524631.3:c.3062T= XP_011522933.1:p.Ile1021=
XM_011524632.3:c.2024T= XP_011522934.1:p.Ile675=
XM_017024488.2:c.3062T= XP_016879977.1:p.Ile1021=
NM_001193466.2:c.3254T= NP_001180395.1:p.Ile1085=
NM_015443.4:c.3254T= MANE Select NP_056258.1:p.Ile1085=
NM_001193465.2:c.3251T= NP_001180394.1:p.Ile1084=
NM_001379198.1:c.3254T= NP_001366127.1:p.Ile1085=