Canonical Allele Identifier: CA382805020
Gene: KMT2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118503191A>T , CM000673.2:g.118503191A>T GRCh38
NC_000011.9:g.118373906A>T , CM000673.1:g.118373906A>T GRCh37
NC_000011.8:g.117879116A>T NCBI36
NG_027813.1:g.71702A>T , LRG_613:g.71702A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000531904.7:c.7398A>T ENSP00000432391.3:p.Lys2466Asn
ENST00000710560.1:c.7389A>T ENSP00000518343.1:p.Lys2463Asn
ENST00000649878.2:c.1338A>T ENSP00000497891.2:p.Lys446Asn
ENST00000685397.1:c.1338A>T ENSP00000509586.1:p.Lys446Asn
ENST00000686370.1:c.1338A>T ENSP00000509179.1:p.Lys446Asn
ENST00000689424.1:c.1596A>T ENSP00000509852.1:p.Lys532Asn
ENST00000691053.1:c.7371A>T ENSP00000509168.1:p.Lys2457Asn
ENST00000389506.10:c.7290A>T ENSP00000374157.5:p.Lys2430Asn
ENST00000528278.2:n.6641A>T
ENST00000534358.8:c.7299A>T MANE Select ENSP00000436786.2:p.Lys2433Asn
ENST00000649699.1:c.7176A>T ENSP00000496927.1:p.Lys2392Asn
ENST00000389506.9:c.7290A>T ENSP00000374157.5:p.Lys2430Asn
ENST00000528278.1:n.1426A>T
ENST00000534358.5:c.7299A>T ENSP00000436786.1:p.Lys2433Asn
NM_001197104.1:c.7299A>T , LRG_613t1:c.7299A>T NP_001184033.1:p.Lys2433Asn
NM_005933.3:c.7290A>T NP_005924.2:p.Lys2430Asn
XM_006718839.2:c.4782A>T XP_006718902.2:p.Lys1594Asn
XM_011542829.1:c.7398A>T XP_011541131.1:p.Lys2466Asn
XM_011542830.1:c.7395A>T XP_011541132.1:p.Lys2465Asn
XM_011542831.1:c.7389A>T XP_011541133.1:p.Lys2463Asn
XM_011542832.1:c.5205A>T XP_011541134.1:p.Lys1735Asn
XM_011542833.1:c.4881A>T XP_011541135.1:p.Lys1627Asn
XM_006718839.3:c.4782A>T XP_006718902.2:p.Lys1594Asn
XM_011542829.2:c.7398A>T XP_011541131.1:p.Lys2466Asn
XM_011542830.2:c.7395A>T XP_011541132.1:p.Lys2465Asn
XM_011542831.2:c.7389A>T XP_011541133.1:p.Lys2463Asn
XM_011542833.2:c.4881A>T XP_011541135.1:p.Lys1627Asn
NM_001197104.2:c.7299A>T MANE Select NP_001184033.1:p.Lys2433Asn
NM_005933.4:c.7290A>T NP_005924.2:p.Lys2430Asn