Canonical Allele Identifier: CA2003527401

Gene: KMT2A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503112T= , CM000673.2:g.118503112T=	GRCh38
NC_000011.9:g.118373827T= , CM000673.1:g.118373827T=	GRCh37
NC_000011.8:g.117879037T=	NCBI36
NG_027813.1:g.71623T= , LRG_613:g.71623T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7319T=	ENSP00000432391.3:p.Leu2440=
ENST00000710560.1:c.7310T=	ENSP00000518343.1:p.Leu2437=
ENST00000649878.2:c.1259T=	ENSP00000497891.2:p.Leu420=
ENST00000685397.1:c.1259T=	ENSP00000509586.1:p.Leu420=
ENST00000686370.1:c.1259T=	ENSP00000509179.1:p.Leu420=
ENST00000689424.1:c.1517T=	ENSP00000509852.1:p.Leu506=
ENST00000691053.1:c.7292T=	ENSP00000509168.1:p.Leu2431=
ENST00000389506.10:c.7211T=	ENSP00000374157.5:p.Leu2404=
ENST00000528278.2:n.6562T=
ENST00000534358.8:c.7220T= MANE Select	ENSP00000436786.2:p.Leu2407=
ENST00000649699.1:c.7097T=	ENSP00000496927.1:p.Leu2366=
ENST00000389506.9:c.7211T=	ENSP00000374157.5:p.Leu2404=
ENST00000528278.1:n.1347T=
ENST00000534358.5:c.7220T=	ENSP00000436786.1:p.Leu2407=
NM_001197104.1:c.7220T= , LRG_613t1:c.7220T=	NP_001184033.1:p.Leu2407=
NM_005933.3:c.7211T=	NP_005924.2:p.Leu2404=
XM_006718839.2:c.4703T=	XP_006718902.2:p.Leu1568=
XM_011542829.1:c.7319T=	XP_011541131.1:p.Leu2440=
XM_011542830.1:c.7316T=	XP_011541132.1:p.Leu2439=
XM_011542831.1:c.7310T=	XP_011541133.1:p.Leu2437=
XM_011542832.1:c.5126T=	XP_011541134.1:p.Leu1709=
XM_011542833.1:c.4802T=	XP_011541135.1:p.Leu1601=
XM_006718839.3:c.4703T=	XP_006718902.2:p.Leu1568=
XM_011542829.2:c.7319T=	XP_011541131.1:p.Leu2440=
XM_011542830.2:c.7316T=	XP_011541132.1:p.Leu2439=
XM_011542831.2:c.7310T=	XP_011541133.1:p.Leu2437=
XM_011542833.2:c.4802T=	XP_011541135.1:p.Leu1601=
NM_001197104.2:c.7220T= MANE Select	NP_001184033.1:p.Leu2407=
NM_005933.4:c.7211T=	NP_005924.2:p.Leu2404=