Canonical Allele Identifier: CA382802981
Gene: KMT2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118502670G>A , CM000673.2:g.118502670G>A GRCh38
NC_000011.9:g.118373385G>A , CM000673.1:g.118373385G>A GRCh37
NC_000011.8:g.117878595G>A NCBI36
NG_027813.1:g.71181G>A , LRG_613:g.71181G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000531904.7:c.6877G>A ENSP00000432391.3:p.Gly2293Arg
ENST00000710560.1:c.6868G>A ENSP00000518343.1:p.Gly2290Arg
ENST00000649878.2:c.817G>A ENSP00000497891.2:p.Gly273Arg
ENST00000685397.1:c.817G>A ENSP00000509586.1:p.Gly273Arg
ENST00000686370.1:c.817G>A ENSP00000509179.1:p.Gly273Arg
ENST00000689424.1:c.1075G>A ENSP00000509852.1:p.Gly359Arg
ENST00000691053.1:c.6850G>A ENSP00000509168.1:p.Gly2284Arg
ENST00000389506.10:c.6769G>A ENSP00000374157.5:p.Gly2257Arg
ENST00000528278.2:n.6120G>A
ENST00000534358.8:c.6778G>A MANE Select ENSP00000436786.2:p.Gly2260Arg
ENST00000649699.1:c.6655G>A ENSP00000496927.1:p.Gly2219Arg
ENST00000389506.9:c.6769G>A ENSP00000374157.5:p.Gly2257Arg
ENST00000528278.1:n.905G>A
ENST00000534358.5:c.6778G>A ENSP00000436786.1:p.Gly2260Arg
NM_001197104.1:c.6778G>A , LRG_613t1:c.6778G>A NP_001184033.1:p.Gly2260Arg
NM_005933.3:c.6769G>A NP_005924.2:p.Gly2257Arg
XM_006718839.2:c.4261G>A XP_006718902.2:p.Gly1421Arg
XM_011542829.1:c.6877G>A XP_011541131.1:p.Gly2293Arg
XM_011542830.1:c.6874G>A XP_011541132.1:p.Gly2292Arg
XM_011542831.1:c.6868G>A XP_011541133.1:p.Gly2290Arg
XM_011542832.1:c.4684G>A XP_011541134.1:p.Gly1562Arg
XM_011542833.1:c.4360G>A XP_011541135.1:p.Gly1454Arg
XM_006718839.3:c.4261G>A XP_006718902.2:p.Gly1421Arg
XM_011542829.2:c.6877G>A XP_011541131.1:p.Gly2293Arg
XM_011542830.2:c.6874G>A XP_011541132.1:p.Gly2292Arg
XM_011542831.2:c.6868G>A XP_011541133.1:p.Gly2290Arg
XM_011542833.2:c.4360G>A XP_011541135.1:p.Gly1454Arg
NM_001197104.2:c.6778G>A MANE Select NP_001184033.1:p.Gly2260Arg
NM_005933.4:c.6769G>A NP_005924.2:p.Gly2257Arg