Canonical Allele Identifier: CA382804887
Gene: KMT2A HGNC NCBI

Linked Data

dbSNP Id: rs2134390780

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118503157G>A , CM000673.2:g.118503157G>A GRCh38
NC_000011.9:g.118373872G>A , CM000673.1:g.118373872G>A GRCh37
NC_000011.8:g.117879082G>A NCBI36
NG_027813.1:g.71668G>A , LRG_613:g.71668G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000531904.7:c.7364G>A ENSP00000432391.3:p.Gly2455Glu
ENST00000710560.1:c.7355G>A ENSP00000518343.1:p.Gly2452Glu
ENST00000649878.2:c.1304G>A ENSP00000497891.2:p.Gly435Glu
ENST00000685397.1:c.1304G>A ENSP00000509586.1:p.Gly435Glu
ENST00000686370.1:c.1304G>A ENSP00000509179.1:p.Gly435Glu
ENST00000689424.1:c.1562G>A ENSP00000509852.1:p.Gly521Glu
ENST00000691053.1:c.7337G>A ENSP00000509168.1:p.Gly2446Glu
ENST00000389506.10:c.7256G>A ENSP00000374157.5:p.Gly2419Glu
ENST00000528278.2:n.6607G>A
ENST00000534358.8:c.7265G>A MANE Select ENSP00000436786.2:p.Gly2422Glu
ENST00000649699.1:c.7142G>A ENSP00000496927.1:p.Gly2381Glu
ENST00000389506.9:c.7256G>A ENSP00000374157.5:p.Gly2419Glu
ENST00000528278.1:n.1392G>A
ENST00000534358.5:c.7265G>A ENSP00000436786.1:p.Gly2422Glu
NM_001197104.1:c.7265G>A , LRG_613t1:c.7265G>A NP_001184033.1:p.Gly2422Glu
NM_005933.3:c.7256G>A NP_005924.2:p.Gly2419Glu
XM_006718839.2:c.4748G>A XP_006718902.2:p.Gly1583Glu
XM_011542829.1:c.7364G>A XP_011541131.1:p.Gly2455Glu
XM_011542830.1:c.7361G>A XP_011541132.1:p.Gly2454Glu
XM_011542831.1:c.7355G>A XP_011541133.1:p.Gly2452Glu
XM_011542832.1:c.5171G>A XP_011541134.1:p.Gly1724Glu
XM_011542833.1:c.4847G>A XP_011541135.1:p.Gly1616Glu
XM_006718839.3:c.4748G>A XP_006718902.2:p.Gly1583Glu
XM_011542829.2:c.7364G>A XP_011541131.1:p.Gly2455Glu
XM_011542830.2:c.7361G>A XP_011541132.1:p.Gly2454Glu
XM_011542831.2:c.7355G>A XP_011541133.1:p.Gly2452Glu
XM_011542833.2:c.4847G>A XP_011541135.1:p.Gly1616Glu
NM_001197104.2:c.7265G>A MANE Select NP_001184033.1:p.Gly2422Glu
NM_005933.4:c.7256G>A NP_005924.2:p.Gly2419Glu