Canonical Allele Identifier: CA2003527594

Gene: KMT2A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503220A= , CM000673.2:g.118503220A=	GRCh38
NC_000011.9:g.118373935A= , CM000673.1:g.118373935A=	GRCh37
NC_000011.8:g.117879145A=	NCBI36
NG_027813.1:g.71731A= , LRG_613:g.71731A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7427A=	ENSP00000432391.3:p.Lys2476=
ENST00000710560.1:c.7418A=	ENSP00000518343.1:p.Lys2473=
ENST00000649878.2:c.1367A=	ENSP00000497891.2:p.Lys456=
ENST00000685397.1:c.1367A=	ENSP00000509586.1:p.Lys456=
ENST00000686370.1:c.1367A=	ENSP00000509179.1:p.Lys456=
ENST00000689424.1:c.1625A=	ENSP00000509852.1:p.Lys542=
ENST00000691053.1:c.7400A=	ENSP00000509168.1:p.Lys2467=
ENST00000389506.10:c.7319A=	ENSP00000374157.5:p.Lys2440=
ENST00000528278.2:n.6670A=
ENST00000534358.8:c.7328A= MANE Select	ENSP00000436786.2:p.Lys2443=
ENST00000649699.1:c.7205A=	ENSP00000496927.1:p.Lys2402=
ENST00000389506.9:c.7319A=	ENSP00000374157.5:p.Lys2440=
ENST00000528278.1:n.1455A=
ENST00000534358.5:c.7328A=	ENSP00000436786.1:p.Lys2443=
NM_001197104.1:c.7328A= , LRG_613t1:c.7328A=	NP_001184033.1:p.Lys2443=
NM_005933.3:c.7319A=	NP_005924.2:p.Lys2440=
XM_006718839.2:c.4811A=	XP_006718902.2:p.Lys1604=
XM_011542829.1:c.7427A=	XP_011541131.1:p.Lys2476=
XM_011542830.1:c.7424A=	XP_011541132.1:p.Lys2475=
XM_011542831.1:c.7418A=	XP_011541133.1:p.Lys2473=
XM_011542832.1:c.5234A=	XP_011541134.1:p.Lys1745=
XM_011542833.1:c.4910A=	XP_011541135.1:p.Lys1637=
XM_006718839.3:c.4811A=	XP_006718902.2:p.Lys1604=
XM_011542829.2:c.7427A=	XP_011541131.1:p.Lys2476=
XM_011542830.2:c.7424A=	XP_011541132.1:p.Lys2475=
XM_011542831.2:c.7418A=	XP_011541133.1:p.Lys2473=
XM_011542833.2:c.4910A=	XP_011541135.1:p.Lys1637=
NM_001197104.2:c.7328A= MANE Select	NP_001184033.1:p.Lys2443=
NM_005933.4:c.7319A=	NP_005924.2:p.Lys2440=