Canonical Allele Identifier: CA382802616
Gene: KMT2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118502560C>G , CM000673.2:g.118502560C>G GRCh38
NC_000011.9:g.118373275C>G , CM000673.1:g.118373275C>G GRCh37
NC_000011.8:g.117878485C>G NCBI36
NG_027813.1:g.71071C>G , LRG_613:g.71071C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000531904.7:c.6767C>G ENSP00000432391.3:p.Ser2256Cys
ENST00000710560.1:c.6758C>G ENSP00000518343.1:p.Ser2253Cys
ENST00000649878.2:c.707C>G ENSP00000497891.2:p.Ser236Cys
ENST00000685397.1:c.707C>G ENSP00000509586.1:p.Ser236Cys
ENST00000686370.1:c.707C>G ENSP00000509179.1:p.Ser236Cys
ENST00000689424.1:c.965C>G ENSP00000509852.1:p.Ser322Cys
ENST00000691053.1:c.6740C>G ENSP00000509168.1:p.Ser2247Cys
ENST00000389506.10:c.6659C>G ENSP00000374157.5:p.Ser2220Cys
ENST00000528278.2:n.6010C>G
ENST00000534358.8:c.6668C>G MANE Select ENSP00000436786.2:p.Ser2223Cys
ENST00000649699.1:c.6545C>G ENSP00000496927.1:p.Ser2182Cys
ENST00000389506.9:c.6659C>G ENSP00000374157.5:p.Ser2220Cys
ENST00000528278.1:n.795C>G
ENST00000534358.5:c.6668C>G ENSP00000436786.1:p.Ser2223Cys
NM_001197104.1:c.6668C>G , LRG_613t1:c.6668C>G NP_001184033.1:p.Ser2223Cys
NM_005933.3:c.6659C>G NP_005924.2:p.Ser2220Cys
XM_006718839.2:c.4151C>G XP_006718902.2:p.Ser1384Cys
XM_011542829.1:c.6767C>G XP_011541131.1:p.Ser2256Cys
XM_011542830.1:c.6764C>G XP_011541132.1:p.Ser2255Cys
XM_011542831.1:c.6758C>G XP_011541133.1:p.Ser2253Cys
XM_011542832.1:c.4574C>G XP_011541134.1:p.Ser1525Cys
XM_011542833.1:c.4250C>G XP_011541135.1:p.Ser1417Cys
XM_006718839.3:c.4151C>G XP_006718902.2:p.Ser1384Cys
XM_011542829.2:c.6767C>G XP_011541131.1:p.Ser2256Cys
XM_011542830.2:c.6764C>G XP_011541132.1:p.Ser2255Cys
XM_011542831.2:c.6758C>G XP_011541133.1:p.Ser2253Cys
XM_011542833.2:c.4250C>G XP_011541135.1:p.Ser1417Cys
NM_001197104.2:c.6668C>G MANE Select NP_001184033.1:p.Ser2223Cys
NM_005933.4:c.6659C>G NP_005924.2:p.Ser2220Cys