Canonical Allele Identifier: CA2003527407

Gene: KMT2A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503115C= , CM000673.2:g.118503115C=	GRCh38
NC_000011.9:g.118373830C= , CM000673.1:g.118373830C=	GRCh37
NC_000011.8:g.117879040C=	NCBI36
NG_027813.1:g.71626C= , LRG_613:g.71626C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7322C=	ENSP00000432391.3:p.Ser2441=
ENST00000710560.1:c.7313C=	ENSP00000518343.1:p.Ser2438=
ENST00000649878.2:c.1262C=	ENSP00000497891.2:p.Ser421=
ENST00000685397.1:c.1262C=	ENSP00000509586.1:p.Ser421=
ENST00000686370.1:c.1262C=	ENSP00000509179.1:p.Ser421=
ENST00000689424.1:c.1520C=	ENSP00000509852.1:p.Ser507=
ENST00000691053.1:c.7295C=	ENSP00000509168.1:p.Ser2432=
ENST00000389506.10:c.7214C=	ENSP00000374157.5:p.Ser2405=
ENST00000528278.2:n.6565C=
ENST00000534358.8:c.7223C= MANE Select	ENSP00000436786.2:p.Ser2408=
ENST00000649699.1:c.7100C=	ENSP00000496927.1:p.Ser2367=
ENST00000389506.9:c.7214C=	ENSP00000374157.5:p.Ser2405=
ENST00000528278.1:n.1350C=
ENST00000534358.5:c.7223C=	ENSP00000436786.1:p.Ser2408=
NM_001197104.1:c.7223C= , LRG_613t1:c.7223C=	NP_001184033.1:p.Ser2408=
NM_005933.3:c.7214C=	NP_005924.2:p.Ser2405=
XM_006718839.2:c.4706C=	XP_006718902.2:p.Ser1569=
XM_011542829.1:c.7322C=	XP_011541131.1:p.Ser2441=
XM_011542830.1:c.7319C=	XP_011541132.1:p.Ser2440=
XM_011542831.1:c.7313C=	XP_011541133.1:p.Ser2438=
XM_011542832.1:c.5129C=	XP_011541134.1:p.Ser1710=
XM_011542833.1:c.4805C=	XP_011541135.1:p.Ser1602=
XM_006718839.3:c.4706C=	XP_006718902.2:p.Ser1569=
XM_011542829.2:c.7322C=	XP_011541131.1:p.Ser2441=
XM_011542830.2:c.7319C=	XP_011541132.1:p.Ser2440=
XM_011542831.2:c.7313C=	XP_011541133.1:p.Ser2438=
XM_011542833.2:c.4805C=	XP_011541135.1:p.Ser1602=
NM_001197104.2:c.7223C= MANE Select	NP_001184033.1:p.Ser2408=
NM_005933.4:c.7214C=	NP_005924.2:p.Ser2405=