Canonical Allele Identifier: CA382804779
Gene: KMT2A HGNC NCBI

Linked Data

dbSNP Id: rs2134390361

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118503121T>G , CM000673.2:g.118503121T>G GRCh38
NC_000011.9:g.118373836T>G , CM000673.1:g.118373836T>G GRCh37
NC_000011.8:g.117879046T>G NCBI36
NG_027813.1:g.71632T>G , LRG_613:g.71632T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000531904.7:c.7328T>G ENSP00000432391.3:p.Met2443Arg
ENST00000710560.1:c.7319T>G ENSP00000518343.1:p.Met2440Arg
ENST00000649878.2:c.1268T>G ENSP00000497891.2:p.Met423Arg
ENST00000685397.1:c.1268T>G ENSP00000509586.1:p.Met423Arg
ENST00000686370.1:c.1268T>G ENSP00000509179.1:p.Met423Arg
ENST00000689424.1:c.1526T>G ENSP00000509852.1:p.Met509Arg
ENST00000691053.1:c.7301T>G ENSP00000509168.1:p.Met2434Arg
ENST00000389506.10:c.7220T>G ENSP00000374157.5:p.Met2407Arg
ENST00000528278.2:n.6571T>G
ENST00000534358.8:c.7229T>G MANE Select ENSP00000436786.2:p.Met2410Arg
ENST00000649699.1:c.7106T>G ENSP00000496927.1:p.Met2369Arg
ENST00000389506.9:c.7220T>G ENSP00000374157.5:p.Met2407Arg
ENST00000528278.1:n.1356T>G
ENST00000534358.5:c.7229T>G ENSP00000436786.1:p.Met2410Arg
NM_001197104.1:c.7229T>G , LRG_613t1:c.7229T>G NP_001184033.1:p.Met2410Arg
NM_005933.3:c.7220T>G NP_005924.2:p.Met2407Arg
XM_006718839.2:c.4712T>G XP_006718902.2:p.Met1571Arg
XM_011542829.1:c.7328T>G XP_011541131.1:p.Met2443Arg
XM_011542830.1:c.7325T>G XP_011541132.1:p.Met2442Arg
XM_011542831.1:c.7319T>G XP_011541133.1:p.Met2440Arg
XM_011542832.1:c.5135T>G XP_011541134.1:p.Met1712Arg
XM_011542833.1:c.4811T>G XP_011541135.1:p.Met1604Arg
XM_006718839.3:c.4712T>G XP_006718902.2:p.Met1571Arg
XM_011542829.2:c.7328T>G XP_011541131.1:p.Met2443Arg
XM_011542830.2:c.7325T>G XP_011541132.1:p.Met2442Arg
XM_011542831.2:c.7319T>G XP_011541133.1:p.Met2440Arg
XM_011542833.2:c.4811T>G XP_011541135.1:p.Met1604Arg
NM_001197104.2:c.7229T>G MANE Select NP_001184033.1:p.Met2410Arg
NM_005933.4:c.7220T>G NP_005924.2:p.Met2407Arg