Canonical Allele Identifier: CA2003527671

Gene: KMT2A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503275A= , CM000673.2:g.118503275A=	GRCh38
NC_000011.9:g.118373990A= , CM000673.1:g.118373990A=	GRCh37
NC_000011.8:g.117879200A=	NCBI36
NG_027813.1:g.71786A= , LRG_613:g.71786A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7482A=	ENSP00000432391.3:p.Gly2494=
ENST00000710560.1:c.7473A=	ENSP00000518343.1:p.Gly2491=
ENST00000649878.2:c.1422A=	ENSP00000497891.2:p.Gly474=
ENST00000685397.1:c.1422A=	ENSP00000509586.1:p.Gly474=
ENST00000686370.1:c.1422A=	ENSP00000509179.1:p.Gly474=
ENST00000689424.1:c.1680A=	ENSP00000509852.1:p.Gly560=
ENST00000691053.1:c.7455A=	ENSP00000509168.1:p.Gly2485=
ENST00000389506.10:c.7374A=	ENSP00000374157.5:p.Gly2458=
ENST00000528278.2:n.6725A=
ENST00000534358.8:c.7383A= MANE Select	ENSP00000436786.2:p.Gly2461=
ENST00000649699.1:c.7260A=	ENSP00000496927.1:p.Gly2420=
ENST00000389506.9:c.7374A=	ENSP00000374157.5:p.Gly2458=
ENST00000528278.1:n.1510A=
ENST00000534358.5:c.7383A=	ENSP00000436786.1:p.Gly2461=
NM_001197104.1:c.7383A= , LRG_613t1:c.7383A=	NP_001184033.1:p.Gly2461=
NM_005933.3:c.7374A=	NP_005924.2:p.Gly2458=
XM_006718839.2:c.4866A=	XP_006718902.2:p.Gly1622=
XM_011542829.1:c.7482A=	XP_011541131.1:p.Gly2494=
XM_011542830.1:c.7479A=	XP_011541132.1:p.Gly2493=
XM_011542831.1:c.7473A=	XP_011541133.1:p.Gly2491=
XM_011542832.1:c.5289A=	XP_011541134.1:p.Gly1763=
XM_011542833.1:c.4965A=	XP_011541135.1:p.Gly1655=
XM_006718839.3:c.4866A=	XP_006718902.2:p.Gly1622=
XM_011542829.2:c.7482A=	XP_011541131.1:p.Gly2494=
XM_011542830.2:c.7479A=	XP_011541132.1:p.Gly2493=
XM_011542831.2:c.7473A=	XP_011541133.1:p.Gly2491=
XM_011542833.2:c.4965A=	XP_011541135.1:p.Gly1655=
NM_001197104.2:c.7383A= MANE Select	NP_001184033.1:p.Gly2461=
NM_005933.4:c.7374A=	NP_005924.2:p.Gly2458=