Canonical Allele Identifier: CA382804869
Gene: KMT2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118503151A>G , CM000673.2:g.118503151A>G GRCh38
NC_000011.9:g.118373866A>G , CM000673.1:g.118373866A>G GRCh37
NC_000011.8:g.117879076A>G NCBI36
NG_027813.1:g.71662A>G , LRG_613:g.71662A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000531904.7:c.7358A>G ENSP00000432391.3:p.His2453Arg
ENST00000710560.1:c.7349A>G ENSP00000518343.1:p.His2450Arg
ENST00000649878.2:c.1298A>G ENSP00000497891.2:p.His433Arg
ENST00000685397.1:c.1298A>G ENSP00000509586.1:p.His433Arg
ENST00000686370.1:c.1298A>G ENSP00000509179.1:p.His433Arg
ENST00000689424.1:c.1556A>G ENSP00000509852.1:p.His519Arg
ENST00000691053.1:c.7331A>G ENSP00000509168.1:p.His2444Arg
ENST00000389506.10:c.7250A>G ENSP00000374157.5:p.His2417Arg
ENST00000528278.2:n.6601A>G
ENST00000534358.8:c.7259A>G MANE Select ENSP00000436786.2:p.His2420Arg
ENST00000649699.1:c.7136A>G ENSP00000496927.1:p.His2379Arg
ENST00000389506.9:c.7250A>G ENSP00000374157.5:p.His2417Arg
ENST00000528278.1:n.1386A>G
ENST00000534358.5:c.7259A>G ENSP00000436786.1:p.His2420Arg
NM_001197104.1:c.7259A>G , LRG_613t1:c.7259A>G NP_001184033.1:p.His2420Arg
NM_005933.3:c.7250A>G NP_005924.2:p.His2417Arg
XM_006718839.2:c.4742A>G XP_006718902.2:p.His1581Arg
XM_011542829.1:c.7358A>G XP_011541131.1:p.His2453Arg
XM_011542830.1:c.7355A>G XP_011541132.1:p.His2452Arg
XM_011542831.1:c.7349A>G XP_011541133.1:p.His2450Arg
XM_011542832.1:c.5165A>G XP_011541134.1:p.His1722Arg
XM_011542833.1:c.4841A>G XP_011541135.1:p.His1614Arg
XM_006718839.3:c.4742A>G XP_006718902.2:p.His1581Arg
XM_011542829.2:c.7358A>G XP_011541131.1:p.His2453Arg
XM_011542830.2:c.7355A>G XP_011541132.1:p.His2452Arg
XM_011542831.2:c.7349A>G XP_011541133.1:p.His2450Arg
XM_011542833.2:c.4841A>G XP_011541135.1:p.His1614Arg
NM_001197104.2:c.7259A>G MANE Select NP_001184033.1:p.His2420Arg
NM_005933.4:c.7250A>G NP_005924.2:p.His2417Arg