Canonical Allele Identifier: CA2003527682

Gene: KMT2A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503290G= , CM000673.2:g.118503290G=	GRCh38
NC_000011.9:g.118374005G= , CM000673.1:g.118374005G=	GRCh37
NC_000011.8:g.117879215G=	NCBI36
NG_027813.1:g.71801G= , LRG_613:g.71801G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7497G=	ENSP00000432391.3:p.Glu2499=
ENST00000710560.1:c.7488G=	ENSP00000518343.1:p.Glu2496=
ENST00000649878.2:c.1437G=	ENSP00000497891.2:p.Glu479=
ENST00000685397.1:c.1437G=	ENSP00000509586.1:p.Glu479=
ENST00000686370.1:c.1437G=	ENSP00000509179.1:p.Glu479=
ENST00000689424.1:c.1695G=	ENSP00000509852.1:p.Glu565=
ENST00000691053.1:c.7470G=	ENSP00000509168.1:p.Glu2490=
ENST00000389506.10:c.7389G=	ENSP00000374157.5:p.Glu2463=
ENST00000528278.2:n.6740G=
ENST00000534358.8:c.7398G= MANE Select	ENSP00000436786.2:p.Glu2466=
ENST00000649699.1:c.7275G=	ENSP00000496927.1:p.Glu2425=
ENST00000389506.9:c.7389G=	ENSP00000374157.5:p.Glu2463=
ENST00000528278.1:n.1525G=
ENST00000534358.5:c.7398G=	ENSP00000436786.1:p.Glu2466=
NM_001197104.1:c.7398G= , LRG_613t1:c.7398G=	NP_001184033.1:p.Glu2466=
NM_005933.3:c.7389G=	NP_005924.2:p.Glu2463=
XM_006718839.2:c.4881G=	XP_006718902.2:p.Glu1627=
XM_011542829.1:c.7497G=	XP_011541131.1:p.Glu2499=
XM_011542830.1:c.7494G=	XP_011541132.1:p.Glu2498=
XM_011542831.1:c.7488G=	XP_011541133.1:p.Glu2496=
XM_011542832.1:c.5304G=	XP_011541134.1:p.Glu1768=
XM_011542833.1:c.4980G=	XP_011541135.1:p.Glu1660=
XM_006718839.3:c.4881G=	XP_006718902.2:p.Glu1627=
XM_011542829.2:c.7497G=	XP_011541131.1:p.Glu2499=
XM_011542830.2:c.7494G=	XP_011541132.1:p.Glu2498=
XM_011542831.2:c.7488G=	XP_011541133.1:p.Glu2496=
XM_011542833.2:c.4980G=	XP_011541135.1:p.Glu1660=
NM_001197104.2:c.7398G= MANE Select	NP_001184033.1:p.Glu2466=
NM_005933.4:c.7389G=	NP_005924.2:p.Glu2463=