Canonical Allele Identifier: CA382826294
Gene: KMT2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118480188A>T , CM000673.2:g.118480188A>T GRCh38
NC_000011.9:g.118350903A>T , CM000673.1:g.118350903A>T GRCh37
NC_000011.8:g.117856113A>T NCBI36
NG_027813.1:g.48699A>T , LRG_613:g.48699A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000531904.7:c.3683A>T ENSP00000432391.3:p.Gln1228Leu
ENST00000710560.1:c.3683A>T ENSP00000518343.1:p.Gln1228Leu
ENST00000527869.7:c.1166A>T ENSP00000432652.3:p.Gln389Leu
ENST00000533790.3:c.1067A>T ENSP00000436700.3:p.Gln356Leu
ENST00000649690.2:c.1391A>T ENSP00000497372.2:p.Gln464Leu
ENST00000685719.1:c.565A>T
ENST00000691053.1:c.3584A>T ENSP00000509168.1:p.Gln1195Leu
ENST00000389506.10:c.3584A>T ENSP00000374157.5:p.Gln1195Leu
ENST00000533790.2:c.836A>T ENSP00000436700.2:p.Gln279Leu
ENST00000534358.8:c.3584A>T MANE Select ENSP00000436786.2:p.Gln1195Leu
ENST00000648261.1:c.2354A>T ENSP00000498126.1:p.Gln785Leu
ENST00000649699.1:c.3584A>T ENSP00000496927.1:p.Gln1195Leu
ENST00000389506.9:c.3584A>T ENSP00000374157.5:p.Gln1195Leu
ENST00000531904.6:c.3683A>T ENSP00000432391.2:p.Gln1228Leu
ENST00000534358.5:c.3584A>T ENSP00000436786.1:p.Gln1195Leu
NM_001197104.1:c.3584A>T , LRG_613t1:c.3584A>T NP_001184033.1:p.Gln1195Leu
NM_005933.3:c.3584A>T NP_005924.2:p.Gln1195Leu
XM_006718839.2:c.1067A>T XP_006718902.2:p.Gln356Leu
XM_011542829.1:c.3683A>T XP_011541131.1:p.Gln1228Leu
XM_011542830.1:c.3683A>T XP_011541132.1:p.Gln1228Leu
XM_011542831.1:c.3683A>T XP_011541133.1:p.Gln1228Leu
XM_011542832.1:c.1490A>T XP_011541134.1:p.Gln497Leu
XM_011542833.1:c.1166A>T XP_011541135.1:p.Gln389Leu
XM_006718839.3:c.1067A>T XP_006718902.2:p.Gln356Leu
XM_011542829.2:c.3683A>T XP_011541131.1:p.Gln1228Leu
XM_011542830.2:c.3683A>T XP_011541132.1:p.Gln1228Leu
XM_011542831.2:c.3683A>T XP_011541133.1:p.Gln1228Leu
XM_011542833.2:c.1166A>T XP_011541135.1:p.Gln389Leu
NM_001197104.2:c.3584A>T MANE Select NP_001184033.1:p.Gln1195Leu
NM_005933.4:c.3584A>T NP_005924.2:p.Gln1195Leu