Canonical Allele Identifier: CA2003527441

Gene: KMT2A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503130G= , CM000673.2:g.118503130G=	GRCh38
NC_000011.9:g.118373845G= , CM000673.1:g.118373845G=	GRCh37
NC_000011.8:g.117879055G=	NCBI36
NG_027813.1:g.71641G= , LRG_613:g.71641G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7337G=	ENSP00000432391.3:p.Arg2446=
ENST00000710560.1:c.7328G=	ENSP00000518343.1:p.Arg2443=
ENST00000649878.2:c.1277G=	ENSP00000497891.2:p.Arg426=
ENST00000685397.1:c.1277G=	ENSP00000509586.1:p.Arg426=
ENST00000686370.1:c.1277G=	ENSP00000509179.1:p.Arg426=
ENST00000689424.1:c.1535G=	ENSP00000509852.1:p.Arg512=
ENST00000691053.1:c.7310G=	ENSP00000509168.1:p.Arg2437=
ENST00000389506.10:c.7229G=	ENSP00000374157.5:p.Arg2410=
ENST00000528278.2:n.6580G=
ENST00000534358.8:c.7238G= MANE Select	ENSP00000436786.2:p.Arg2413=
ENST00000649699.1:c.7115G=	ENSP00000496927.1:p.Arg2372=
ENST00000389506.9:c.7229G=	ENSP00000374157.5:p.Arg2410=
ENST00000528278.1:n.1365G=
ENST00000534358.5:c.7238G=	ENSP00000436786.1:p.Arg2413=
NM_001197104.1:c.7238G= , LRG_613t1:c.7238G=	NP_001184033.1:p.Arg2413=
NM_005933.3:c.7229G=	NP_005924.2:p.Arg2410=
XM_006718839.2:c.4721G=	XP_006718902.2:p.Arg1574=
XM_011542829.1:c.7337G=	XP_011541131.1:p.Arg2446=
XM_011542830.1:c.7334G=	XP_011541132.1:p.Arg2445=
XM_011542831.1:c.7328G=	XP_011541133.1:p.Arg2443=
XM_011542832.1:c.5144G=	XP_011541134.1:p.Arg1715=
XM_011542833.1:c.4820G=	XP_011541135.1:p.Arg1607=
XM_006718839.3:c.4721G=	XP_006718902.2:p.Arg1574=
XM_011542829.2:c.7337G=	XP_011541131.1:p.Arg2446=
XM_011542830.2:c.7334G=	XP_011541132.1:p.Arg2445=
XM_011542831.2:c.7328G=	XP_011541133.1:p.Arg2443=
XM_011542833.2:c.4820G=	XP_011541135.1:p.Arg1607=
NM_001197104.2:c.7238G= MANE Select	NP_001184033.1:p.Arg2413=
NM_005933.4:c.7229G=	NP_005924.2:p.Arg2410=