Canonical Allele Identifier: CA382805387
Gene: KMT2A HGNC NCBI

Linked Data

dbSNP Id: rs2134391656

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118503286C>G , CM000673.2:g.118503286C>G GRCh38
NC_000011.9:g.118374001C>G , CM000673.1:g.118374001C>G GRCh37
NC_000011.8:g.117879211C>G NCBI36
NG_027813.1:g.71797C>G , LRG_613:g.71797C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000531904.7:c.7493C>G ENSP00000432391.3:p.Pro2498Arg
ENST00000710560.1:c.7484C>G ENSP00000518343.1:p.Pro2495Arg
ENST00000649878.2:c.1433C>G ENSP00000497891.2:p.Pro478Arg
ENST00000685397.1:c.1433C>G ENSP00000509586.1:p.Pro478Arg
ENST00000686370.1:c.1433C>G ENSP00000509179.1:p.Pro478Arg
ENST00000689424.1:c.1691C>G ENSP00000509852.1:p.Pro564Arg
ENST00000691053.1:c.7466C>G ENSP00000509168.1:p.Pro2489Arg
ENST00000389506.10:c.7385C>G ENSP00000374157.5:p.Pro2462Arg
ENST00000528278.2:n.6736C>G
ENST00000534358.8:c.7394C>G MANE Select ENSP00000436786.2:p.Pro2465Arg
ENST00000649699.1:c.7271C>G ENSP00000496927.1:p.Pro2424Arg
ENST00000389506.9:c.7385C>G ENSP00000374157.5:p.Pro2462Arg
ENST00000528278.1:n.1521C>G
ENST00000534358.5:c.7394C>G ENSP00000436786.1:p.Pro2465Arg
NM_001197104.1:c.7394C>G , LRG_613t1:c.7394C>G NP_001184033.1:p.Pro2465Arg
NM_005933.3:c.7385C>G NP_005924.2:p.Pro2462Arg
XM_006718839.2:c.4877C>G XP_006718902.2:p.Pro1626Arg
XM_011542829.1:c.7493C>G XP_011541131.1:p.Pro2498Arg
XM_011542830.1:c.7490C>G XP_011541132.1:p.Pro2497Arg
XM_011542831.1:c.7484C>G XP_011541133.1:p.Pro2495Arg
XM_011542832.1:c.5300C>G XP_011541134.1:p.Pro1767Arg
XM_011542833.1:c.4976C>G XP_011541135.1:p.Pro1659Arg
XM_006718839.3:c.4877C>G XP_006718902.2:p.Pro1626Arg
XM_011542829.2:c.7493C>G XP_011541131.1:p.Pro2498Arg
XM_011542830.2:c.7490C>G XP_011541132.1:p.Pro2497Arg
XM_011542831.2:c.7484C>G XP_011541133.1:p.Pro2495Arg
XM_011542833.2:c.4976C>G XP_011541135.1:p.Pro1659Arg
NM_001197104.2:c.7394C>G MANE Select NP_001184033.1:p.Pro2465Arg
NM_005933.4:c.7385C>G NP_005924.2:p.Pro2462Arg