Canonical Allele Identifier: CA382804977
Gene: KMT2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118503181A>C , CM000673.2:g.118503181A>C GRCh38
NC_000011.9:g.118373896A>C , CM000673.1:g.118373896A>C GRCh37
NC_000011.8:g.117879106A>C NCBI36
NG_027813.1:g.71692A>C , LRG_613:g.71692A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000531904.7:c.7388A>C ENSP00000432391.3:p.Gln2463Pro
ENST00000710560.1:c.7379A>C ENSP00000518343.1:p.Gln2460Pro
ENST00000649878.2:c.1328A>C ENSP00000497891.2:p.Gln443Pro
ENST00000685397.1:c.1328A>C ENSP00000509586.1:p.Gln443Pro
ENST00000686370.1:c.1328A>C ENSP00000509179.1:p.Gln443Pro
ENST00000689424.1:c.1586A>C ENSP00000509852.1:p.Gln529Pro
ENST00000691053.1:c.7361A>C ENSP00000509168.1:p.Gln2454Pro
ENST00000389506.10:c.7280A>C ENSP00000374157.5:p.Gln2427Pro
ENST00000528278.2:n.6631A>C
ENST00000534358.8:c.7289A>C MANE Select ENSP00000436786.2:p.Gln2430Pro
ENST00000649699.1:c.7166A>C ENSP00000496927.1:p.Gln2389Pro
ENST00000389506.9:c.7280A>C ENSP00000374157.5:p.Gln2427Pro
ENST00000528278.1:n.1416A>C
ENST00000534358.5:c.7289A>C ENSP00000436786.1:p.Gln2430Pro
NM_001197104.1:c.7289A>C , LRG_613t1:c.7289A>C NP_001184033.1:p.Gln2430Pro
NM_005933.3:c.7280A>C NP_005924.2:p.Gln2427Pro
XM_006718839.2:c.4772A>C XP_006718902.2:p.Gln1591Pro
XM_011542829.1:c.7388A>C XP_011541131.1:p.Gln2463Pro
XM_011542830.1:c.7385A>C XP_011541132.1:p.Gln2462Pro
XM_011542831.1:c.7379A>C XP_011541133.1:p.Gln2460Pro
XM_011542832.1:c.5195A>C XP_011541134.1:p.Gln1732Pro
XM_011542833.1:c.4871A>C XP_011541135.1:p.Gln1624Pro
XM_006718839.3:c.4772A>C XP_006718902.2:p.Gln1591Pro
XM_011542829.2:c.7388A>C XP_011541131.1:p.Gln2463Pro
XM_011542830.2:c.7385A>C XP_011541132.1:p.Gln2462Pro
XM_011542831.2:c.7379A>C XP_011541133.1:p.Gln2460Pro
XM_011542833.2:c.4871A>C XP_011541135.1:p.Gln1624Pro
NM_001197104.2:c.7289A>C MANE Select NP_001184033.1:p.Gln2430Pro
NM_005933.4:c.7280A>C NP_005924.2:p.Gln2427Pro