Canonical Allele Identifier: CA2003528001

Gene: KMT2A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503554G= , CM000673.2:g.118503554G=	GRCh38
NC_000011.9:g.118374269G= , CM000673.1:g.118374269G=	GRCh37
NC_000011.8:g.117879479G=	NCBI36
NG_027813.1:g.72065G= , LRG_613:g.72065G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000531904.7:c.7761G=	ENSP00000432391.3:p.Glu2587=
ENST00000710560.1:c.7752G=	ENSP00000518343.1:p.Glu2584=
ENST00000649878.2:c.1701G=	ENSP00000497891.2:p.Glu567=
ENST00000685397.1:c.1701G=	ENSP00000509586.1:p.Glu567=
ENST00000686370.1:c.1701G=	ENSP00000509179.1:p.Glu567=
ENST00000689424.1:c.1959G=	ENSP00000509852.1:p.Glu653=
ENST00000691053.1:c.7734G=	ENSP00000509168.1:p.Glu2578=
ENST00000389506.10:c.7653G=	ENSP00000374157.5:p.Glu2551=
ENST00000528278.2:n.7004G=
ENST00000534358.8:c.7662G= MANE Select	ENSP00000436786.2:p.Glu2554=
ENST00000649699.1:c.7539G=	ENSP00000496927.1:p.Glu2513=
ENST00000389506.9:c.7653G=	ENSP00000374157.5:p.Glu2551=
ENST00000528278.1:n.1789G=
ENST00000534358.5:c.7662G=	ENSP00000436786.1:p.Glu2554=
NM_001197104.1:c.7662G= , LRG_613t1:c.7662G=	NP_001184033.1:p.Glu2554=
NM_005933.3:c.7653G=	NP_005924.2:p.Glu2551=
XM_006718839.2:c.5145G=	XP_006718902.2:p.Glu1715=
XM_011542829.1:c.7761G=	XP_011541131.1:p.Glu2587=
XM_011542830.1:c.7758G=	XP_011541132.1:p.Glu2586=
XM_011542831.1:c.7752G=	XP_011541133.1:p.Glu2584=
XM_011542832.1:c.5568G=	XP_011541134.1:p.Glu1856=
XM_011542833.1:c.5244G=	XP_011541135.1:p.Glu1748=
XM_006718839.3:c.5145G=	XP_006718902.2:p.Glu1715=
XM_011542829.2:c.7761G=	XP_011541131.1:p.Glu2587=
XM_011542830.2:c.7758G=	XP_011541132.1:p.Glu2586=
XM_011542831.2:c.7752G=	XP_011541133.1:p.Glu2584=
XM_011542833.2:c.5244G=	XP_011541135.1:p.Glu1748=
NM_001197104.2:c.7662G= MANE Select	NP_001184033.1:p.Glu2554=
NM_005933.4:c.7653G=	NP_005924.2:p.Glu2551=