Canonical Allele Identifier: CA382805523
Gene: KMT2A HGNC NCBI

Linked Data

dbSNP Id: rs1359749720

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118503317G>C , CM000673.2:g.118503317G>C GRCh38
NC_000011.9:g.118374032G>C , CM000673.1:g.118374032G>C GRCh37
NC_000011.8:g.117879242G>C NCBI36
NG_027813.1:g.71828G>C , LRG_613:g.71828G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000531904.7:c.7524G>C ENSP00000432391.3:p.Glu2508Asp
ENST00000710560.1:c.7515G>C ENSP00000518343.1:p.Glu2505Asp
ENST00000649878.2:c.1464G>C ENSP00000497891.2:p.Glu488Asp
ENST00000685397.1:c.1464G>C ENSP00000509586.1:p.Glu488Asp
ENST00000686370.1:c.1464G>C ENSP00000509179.1:p.Glu488Asp
ENST00000689424.1:c.1722G>C ENSP00000509852.1:p.Glu574Asp
ENST00000691053.1:c.7497G>C ENSP00000509168.1:p.Glu2499Asp
ENST00000389506.10:c.7416G>C ENSP00000374157.5:p.Glu2472Asp
ENST00000528278.2:n.6767G>C
ENST00000534358.8:c.7425G>C MANE Select ENSP00000436786.2:p.Glu2475Asp
ENST00000649699.1:c.7302G>C ENSP00000496927.1:p.Glu2434Asp
ENST00000389506.9:c.7416G>C ENSP00000374157.5:p.Glu2472Asp
ENST00000528278.1:n.1552G>C
ENST00000534358.5:c.7425G>C ENSP00000436786.1:p.Glu2475Asp
NM_001197104.1:c.7425G>C , LRG_613t1:c.7425G>C NP_001184033.1:p.Glu2475Asp
NM_005933.3:c.7416G>C NP_005924.2:p.Glu2472Asp
XM_006718839.2:c.4908G>C XP_006718902.2:p.Glu1636Asp
XM_011542829.1:c.7524G>C XP_011541131.1:p.Glu2508Asp
XM_011542830.1:c.7521G>C XP_011541132.1:p.Glu2507Asp
XM_011542831.1:c.7515G>C XP_011541133.1:p.Glu2505Asp
XM_011542832.1:c.5331G>C XP_011541134.1:p.Glu1777Asp
XM_011542833.1:c.5007G>C XP_011541135.1:p.Glu1669Asp
XM_006718839.3:c.4908G>C XP_006718902.2:p.Glu1636Asp
XM_011542829.2:c.7524G>C XP_011541131.1:p.Glu2508Asp
XM_011542830.2:c.7521G>C XP_011541132.1:p.Glu2507Asp
XM_011542831.2:c.7515G>C XP_011541133.1:p.Glu2505Asp
XM_011542833.2:c.5007G>C XP_011541135.1:p.Glu1669Asp
NM_001197104.2:c.7425G>C MANE Select NP_001184033.1:p.Glu2475Asp
NM_005933.4:c.7416G>C NP_005924.2:p.Glu2472Asp