Canonical Allele Identifier: CA2003527569

Gene: KMT2A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503199G= , CM000673.2:g.118503199G=	GRCh38
NC_000011.9:g.118373914G= , CM000673.1:g.118373914G=	GRCh37
NC_000011.8:g.117879124G=	NCBI36
NG_027813.1:g.71710G= , LRG_613:g.71710G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7406G=	ENSP00000432391.3:p.Cys2469=
ENST00000710560.1:c.7397G=	ENSP00000518343.1:p.Cys2466=
ENST00000649878.2:c.1346G=	ENSP00000497891.2:p.Cys449=
ENST00000685397.1:c.1346G=	ENSP00000509586.1:p.Cys449=
ENST00000686370.1:c.1346G=	ENSP00000509179.1:p.Cys449=
ENST00000689424.1:c.1604G=	ENSP00000509852.1:p.Cys535=
ENST00000691053.1:c.7379G=	ENSP00000509168.1:p.Cys2460=
ENST00000389506.10:c.7298G=	ENSP00000374157.5:p.Cys2433=
ENST00000528278.2:n.6649G=
ENST00000534358.8:c.7307G= MANE Select	ENSP00000436786.2:p.Cys2436=
ENST00000649699.1:c.7184G=	ENSP00000496927.1:p.Cys2395=
ENST00000389506.9:c.7298G=	ENSP00000374157.5:p.Cys2433=
ENST00000528278.1:n.1434G=
ENST00000534358.5:c.7307G=	ENSP00000436786.1:p.Cys2436=
NM_001197104.1:c.7307G= , LRG_613t1:c.7307G=	NP_001184033.1:p.Cys2436=
NM_005933.3:c.7298G=	NP_005924.2:p.Cys2433=
XM_006718839.2:c.4790G=	XP_006718902.2:p.Cys1597=
XM_011542829.1:c.7406G=	XP_011541131.1:p.Cys2469=
XM_011542830.1:c.7403G=	XP_011541132.1:p.Cys2468=
XM_011542831.1:c.7397G=	XP_011541133.1:p.Cys2466=
XM_011542832.1:c.5213G=	XP_011541134.1:p.Cys1738=
XM_011542833.1:c.4889G=	XP_011541135.1:p.Cys1630=
XM_006718839.3:c.4790G=	XP_006718902.2:p.Cys1597=
XM_011542829.2:c.7406G=	XP_011541131.1:p.Cys2469=
XM_011542830.2:c.7403G=	XP_011541132.1:p.Cys2468=
XM_011542831.2:c.7397G=	XP_011541133.1:p.Cys2466=
XM_011542833.2:c.4889G=	XP_011541135.1:p.Cys1630=
NM_001197104.2:c.7307G= MANE Select	NP_001184033.1:p.Cys2436=
NM_005933.4:c.7298G=	NP_005924.2:p.Cys2433=