Canonical Allele Identifier: CA382805457
Gene: KMT2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118503300G>T , CM000673.2:g.118503300G>T GRCh38
NC_000011.9:g.118374015G>T , CM000673.1:g.118374015G>T GRCh37
NC_000011.8:g.117879225G>T NCBI36
NG_027813.1:g.71811G>T , LRG_613:g.71811G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000531904.7:c.7507G>T ENSP00000432391.3:p.Glu2503Ter
ENST00000710560.1:c.7498G>T ENSP00000518343.1:p.Glu2500Ter
ENST00000649878.2:c.1447G>T ENSP00000497891.2:p.Glu483Ter
ENST00000685397.1:c.1447G>T ENSP00000509586.1:p.Glu483Ter
ENST00000686370.1:c.1447G>T ENSP00000509179.1:p.Glu483Ter
ENST00000689424.1:c.1705G>T ENSP00000509852.1:p.Glu569Ter
ENST00000691053.1:c.7480G>T ENSP00000509168.1:p.Glu2494Ter
ENST00000389506.10:c.7399G>T ENSP00000374157.5:p.Glu2467Ter
ENST00000528278.2:n.6750G>T
ENST00000534358.8:c.7408G>T MANE Select ENSP00000436786.2:p.Glu2470Ter
ENST00000649699.1:c.7285G>T ENSP00000496927.1:p.Glu2429Ter
ENST00000389506.9:c.7399G>T ENSP00000374157.5:p.Glu2467Ter
ENST00000528278.1:n.1535G>T
ENST00000534358.5:c.7408G>T ENSP00000436786.1:p.Glu2470Ter
NM_001197104.1:c.7408G>T , LRG_613t1:c.7408G>T NP_001184033.1:p.Glu2470Ter
NM_005933.3:c.7399G>T NP_005924.2:p.Glu2467Ter
XM_006718839.2:c.4891G>T XP_006718902.2:p.Glu1631Ter
XM_011542829.1:c.7507G>T XP_011541131.1:p.Glu2503Ter
XM_011542830.1:c.7504G>T XP_011541132.1:p.Glu2502Ter
XM_011542831.1:c.7498G>T XP_011541133.1:p.Glu2500Ter
XM_011542832.1:c.5314G>T XP_011541134.1:p.Glu1772Ter
XM_011542833.1:c.4990G>T XP_011541135.1:p.Glu1664Ter
XM_006718839.3:c.4891G>T XP_006718902.2:p.Glu1631Ter
XM_011542829.2:c.7507G>T XP_011541131.1:p.Glu2503Ter
XM_011542830.2:c.7504G>T XP_011541132.1:p.Glu2502Ter
XM_011542831.2:c.7498G>T XP_011541133.1:p.Glu2500Ter
XM_011542833.2:c.4990G>T XP_011541135.1:p.Glu1664Ter
NM_001197104.2:c.7408G>T MANE Select NP_001184033.1:p.Glu2470Ter
NM_005933.4:c.7399G>T NP_005924.2:p.Glu2467Ter