Canonical Allele Identifier: CA382804901
Gene: KMT2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118503162A>C , CM000673.2:g.118503162A>C GRCh38
NC_000011.9:g.118373877A>C , CM000673.1:g.118373877A>C GRCh37
NC_000011.8:g.117879087A>C NCBI36
NG_027813.1:g.71673A>C , LRG_613:g.71673A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000531904.7:c.7369A>C ENSP00000432391.3:p.Ser2457Arg
ENST00000710560.1:c.7360A>C ENSP00000518343.1:p.Ser2454Arg
ENST00000649878.2:c.1309A>C ENSP00000497891.2:p.Ser437Arg
ENST00000685397.1:c.1309A>C ENSP00000509586.1:p.Ser437Arg
ENST00000686370.1:c.1309A>C ENSP00000509179.1:p.Ser437Arg
ENST00000689424.1:c.1567A>C ENSP00000509852.1:p.Ser523Arg
ENST00000691053.1:c.7342A>C ENSP00000509168.1:p.Ser2448Arg
ENST00000389506.10:c.7261A>C ENSP00000374157.5:p.Ser2421Arg
ENST00000528278.2:n.6612A>C
ENST00000534358.8:c.7270A>C MANE Select ENSP00000436786.2:p.Ser2424Arg
ENST00000649699.1:c.7147A>C ENSP00000496927.1:p.Ser2383Arg
ENST00000389506.9:c.7261A>C ENSP00000374157.5:p.Ser2421Arg
ENST00000528278.1:n.1397A>C
ENST00000534358.5:c.7270A>C ENSP00000436786.1:p.Ser2424Arg
NM_001197104.1:c.7270A>C , LRG_613t1:c.7270A>C NP_001184033.1:p.Ser2424Arg
NM_005933.3:c.7261A>C NP_005924.2:p.Ser2421Arg
XM_006718839.2:c.4753A>C XP_006718902.2:p.Ser1585Arg
XM_011542829.1:c.7369A>C XP_011541131.1:p.Ser2457Arg
XM_011542830.1:c.7366A>C XP_011541132.1:p.Ser2456Arg
XM_011542831.1:c.7360A>C XP_011541133.1:p.Ser2454Arg
XM_011542832.1:c.5176A>C XP_011541134.1:p.Ser1726Arg
XM_011542833.1:c.4852A>C XP_011541135.1:p.Ser1618Arg
XM_006718839.3:c.4753A>C XP_006718902.2:p.Ser1585Arg
XM_011542829.2:c.7369A>C XP_011541131.1:p.Ser2457Arg
XM_011542830.2:c.7366A>C XP_011541132.1:p.Ser2456Arg
XM_011542831.2:c.7360A>C XP_011541133.1:p.Ser2454Arg
XM_011542833.2:c.4852A>C XP_011541135.1:p.Ser1618Arg
NM_001197104.2:c.7270A>C MANE Select NP_001184033.1:p.Ser2424Arg
NM_005933.4:c.7261A>C NP_005924.2:p.Ser2421Arg