Canonical Allele Identifier: CA382805075

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118373920A>T (hg19) ; chr11:g.118503205A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503205A>T , CM000673.2:g.118503205A>T	GRCh38
NC_000011.9:g.118373920A>T , CM000673.1:g.118373920A>T	GRCh37
NC_000011.8:g.117879130A>T	NCBI36
NG_027813.1:g.71716A>T , LRG_613:g.71716A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7412A>T	ENSP00000432391.3:p.Glu2471Val
ENST00000710560.1:c.7403A>T	ENSP00000518343.1:p.Glu2468Val
ENST00000649878.2:c.1352A>T	ENSP00000497891.2:p.Glu451Val
ENST00000685397.1:c.1352A>T	ENSP00000509586.1:p.Glu451Val
ENST00000686370.1:c.1352A>T	ENSP00000509179.1:p.Glu451Val
ENST00000689424.1:c.1610A>T	ENSP00000509852.1:p.Glu537Val
ENST00000691053.1:c.7385A>T	ENSP00000509168.1:p.Glu2462Val
ENST00000389506.10:c.7304A>T	ENSP00000374157.5:p.Glu2435Val
ENST00000528278.2:n.6655A>T
ENST00000534358.8:c.7313A>T MANE Select	ENSP00000436786.2:p.Glu2438Val
ENST00000649699.1:c.7190A>T	ENSP00000496927.1:p.Glu2397Val
ENST00000389506.9:c.7304A>T	ENSP00000374157.5:p.Glu2435Val
ENST00000528278.1:n.1440A>T
ENST00000534358.5:c.7313A>T	ENSP00000436786.1:p.Glu2438Val
NM_001197104.1:c.7313A>T , LRG_613t1:c.7313A>T	NP_001184033.1:p.Glu2438Val
NM_005933.3:c.7304A>T	NP_005924.2:p.Glu2435Val
XM_006718839.2:c.4796A>T	XP_006718902.2:p.Glu1599Val
XM_011542829.1:c.7412A>T	XP_011541131.1:p.Glu2471Val
XM_011542830.1:c.7409A>T	XP_011541132.1:p.Glu2470Val
XM_011542831.1:c.7403A>T	XP_011541133.1:p.Glu2468Val
XM_011542832.1:c.5219A>T	XP_011541134.1:p.Glu1740Val
XM_011542833.1:c.4895A>T	XP_011541135.1:p.Glu1632Val
XM_006718839.3:c.4796A>T	XP_006718902.2:p.Glu1599Val
XM_011542829.2:c.7412A>T	XP_011541131.1:p.Glu2471Val
XM_011542830.2:c.7409A>T	XP_011541132.1:p.Glu2470Val
XM_011542831.2:c.7403A>T	XP_011541133.1:p.Glu2468Val
XM_011542833.2:c.4895A>T	XP_011541135.1:p.Glu1632Val
NM_001197104.2:c.7313A>T MANE Select	NP_001184033.1:p.Glu2438Val
NM_005933.4:c.7304A>T	NP_005924.2:p.Glu2435Val