Canonical Allele Identifier: CA382804884
Gene: KMT2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118503156G>T , CM000673.2:g.118503156G>T GRCh38
NC_000011.9:g.118373871G>T , CM000673.1:g.118373871G>T GRCh37
NC_000011.8:g.117879081G>T NCBI36
NG_027813.1:g.71667G>T , LRG_613:g.71667G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000531904.7:c.7363G>T ENSP00000432391.3:p.Gly2455Ter
ENST00000710560.1:c.7354G>T ENSP00000518343.1:p.Gly2452Ter
ENST00000649878.2:c.1303G>T ENSP00000497891.2:p.Gly435Ter
ENST00000685397.1:c.1303G>T ENSP00000509586.1:p.Gly435Ter
ENST00000686370.1:c.1303G>T ENSP00000509179.1:p.Gly435Ter
ENST00000689424.1:c.1561G>T ENSP00000509852.1:p.Gly521Ter
ENST00000691053.1:c.7336G>T ENSP00000509168.1:p.Gly2446Ter
ENST00000389506.10:c.7255G>T ENSP00000374157.5:p.Gly2419Ter
ENST00000528278.2:n.6606G>T
ENST00000534358.8:c.7264G>T MANE Select ENSP00000436786.2:p.Gly2422Ter
ENST00000649699.1:c.7141G>T ENSP00000496927.1:p.Gly2381Ter
ENST00000389506.9:c.7255G>T ENSP00000374157.5:p.Gly2419Ter
ENST00000528278.1:n.1391G>T
ENST00000534358.5:c.7264G>T ENSP00000436786.1:p.Gly2422Ter
NM_001197104.1:c.7264G>T , LRG_613t1:c.7264G>T NP_001184033.1:p.Gly2422Ter
NM_005933.3:c.7255G>T NP_005924.2:p.Gly2419Ter
XM_006718839.2:c.4747G>T XP_006718902.2:p.Gly1583Ter
XM_011542829.1:c.7363G>T XP_011541131.1:p.Gly2455Ter
XM_011542830.1:c.7360G>T XP_011541132.1:p.Gly2454Ter
XM_011542831.1:c.7354G>T XP_011541133.1:p.Gly2452Ter
XM_011542832.1:c.5170G>T XP_011541134.1:p.Gly1724Ter
XM_011542833.1:c.4846G>T XP_011541135.1:p.Gly1616Ter
XM_006718839.3:c.4747G>T XP_006718902.2:p.Gly1583Ter
XM_011542829.2:c.7363G>T XP_011541131.1:p.Gly2455Ter
XM_011542830.2:c.7360G>T XP_011541132.1:p.Gly2454Ter
XM_011542831.2:c.7354G>T XP_011541133.1:p.Gly2452Ter
XM_011542833.2:c.4846G>T XP_011541135.1:p.Gly1616Ter
NM_001197104.2:c.7264G>T MANE Select NP_001184033.1:p.Gly2422Ter
NM_005933.4:c.7255G>T NP_005924.2:p.Gly2419Ter