Canonical Allele Identifier: CA2003527967

Gene: KMT2A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503523A= , CM000673.2:g.118503523A=	GRCh38
NC_000011.9:g.118374238A= , CM000673.1:g.118374238A=	GRCh37
NC_000011.8:g.117879448A=	NCBI36
NG_027813.1:g.72034A= , LRG_613:g.72034A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7730A=	ENSP00000432391.3:p.Glu2577=
ENST00000710560.1:c.7721A=	ENSP00000518343.1:p.Glu2574=
ENST00000649878.2:c.1670A=	ENSP00000497891.2:p.Glu557=
ENST00000685397.1:c.1670A=	ENSP00000509586.1:p.Glu557=
ENST00000686370.1:c.1670A=	ENSP00000509179.1:p.Glu557=
ENST00000689424.1:c.1928A=	ENSP00000509852.1:p.Glu643=
ENST00000691053.1:c.7703A=	ENSP00000509168.1:p.Glu2568=
ENST00000389506.10:c.7622A=	ENSP00000374157.5:p.Glu2541=
ENST00000528278.2:n.6973A=
ENST00000534358.8:c.7631A= MANE Select	ENSP00000436786.2:p.Glu2544=
ENST00000649699.1:c.7508A=	ENSP00000496927.1:p.Glu2503=
ENST00000389506.9:c.7622A=	ENSP00000374157.5:p.Glu2541=
ENST00000528278.1:n.1758A=
ENST00000534358.5:c.7631A=	ENSP00000436786.1:p.Glu2544=
NM_001197104.1:c.7631A= , LRG_613t1:c.7631A=	NP_001184033.1:p.Glu2544=
NM_005933.3:c.7622A=	NP_005924.2:p.Glu2541=
XM_006718839.2:c.5114A=	XP_006718902.2:p.Glu1705=
XM_011542829.1:c.7730A=	XP_011541131.1:p.Glu2577=
XM_011542830.1:c.7727A=	XP_011541132.1:p.Glu2576=
XM_011542831.1:c.7721A=	XP_011541133.1:p.Glu2574=
XM_011542832.1:c.5537A=	XP_011541134.1:p.Glu1846=
XM_011542833.1:c.5213A=	XP_011541135.1:p.Glu1738=
XM_006718839.3:c.5114A=	XP_006718902.2:p.Glu1705=
XM_011542829.2:c.7730A=	XP_011541131.1:p.Glu2577=
XM_011542830.2:c.7727A=	XP_011541132.1:p.Glu2576=
XM_011542831.2:c.7721A=	XP_011541133.1:p.Glu2574=
XM_011542833.2:c.5213A=	XP_011541135.1:p.Glu1738=
NM_001197104.2:c.7631A= MANE Select	NP_001184033.1:p.Glu2544=
NM_005933.4:c.7622A=	NP_005924.2:p.Glu2541=