Canonical Allele Identifier: CA382802444
Gene: KMT2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118502515C>T , CM000673.2:g.118502515C>T GRCh38
NC_000011.9:g.118373230C>T , CM000673.1:g.118373230C>T GRCh37
NC_000011.8:g.117878440C>T NCBI36
NG_027813.1:g.71026C>T , LRG_613:g.71026C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000531904.7:c.6722C>T ENSP00000432391.3:p.Ser2241Phe
ENST00000710560.1:c.6713C>T ENSP00000518343.1:p.Ser2238Phe
ENST00000649878.2:c.662C>T ENSP00000497891.2:p.Ser221Phe
ENST00000685397.1:c.662C>T ENSP00000509586.1:p.Ser221Phe
ENST00000686370.1:c.662C>T ENSP00000509179.1:p.Ser221Phe
ENST00000689424.1:c.920C>T ENSP00000509852.1:p.Ser307Phe
ENST00000691053.1:c.6695C>T ENSP00000509168.1:p.Ser2232Phe
ENST00000389506.10:c.6614C>T ENSP00000374157.5:p.Ser2205Phe
ENST00000528278.2:n.5965C>T
ENST00000534358.8:c.6623C>T MANE Select ENSP00000436786.2:p.Ser2208Phe
ENST00000649699.1:c.6500C>T ENSP00000496927.1:p.Ser2167Phe
ENST00000389506.9:c.6614C>T ENSP00000374157.5:p.Ser2205Phe
ENST00000528278.1:n.750C>T
ENST00000534358.5:c.6623C>T ENSP00000436786.1:p.Ser2208Phe
NM_001197104.1:c.6623C>T , LRG_613t1:c.6623C>T NP_001184033.1:p.Ser2208Phe
NM_005933.3:c.6614C>T NP_005924.2:p.Ser2205Phe
XM_006718839.2:c.4106C>T XP_006718902.2:p.Ser1369Phe
XM_011542829.1:c.6722C>T XP_011541131.1:p.Ser2241Phe
XM_011542830.1:c.6719C>T XP_011541132.1:p.Ser2240Phe
XM_011542831.1:c.6713C>T XP_011541133.1:p.Ser2238Phe
XM_011542832.1:c.4529C>T XP_011541134.1:p.Ser1510Phe
XM_011542833.1:c.4205C>T XP_011541135.1:p.Ser1402Phe
XM_006718839.3:c.4106C>T XP_006718902.2:p.Ser1369Phe
XM_011542829.2:c.6722C>T XP_011541131.1:p.Ser2241Phe
XM_011542830.2:c.6719C>T XP_011541132.1:p.Ser2240Phe
XM_011542831.2:c.6713C>T XP_011541133.1:p.Ser2238Phe
XM_011542833.2:c.4205C>T XP_011541135.1:p.Ser1402Phe
NM_001197104.2:c.6623C>T MANE Select NP_001184033.1:p.Ser2208Phe
NM_005933.4:c.6614C>T NP_005924.2:p.Ser2205Phe