Canonical Allele Identifier: CA2003527876

Gene: KMT2A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503430A= , CM000673.2:g.118503430A=	GRCh38
NC_000011.9:g.118374145A= , CM000673.1:g.118374145A=	GRCh37
NC_000011.8:g.117879355A=	NCBI36
NG_027813.1:g.71941A= , LRG_613:g.71941A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7637A=	ENSP00000432391.3:p.Lys2546=
ENST00000710560.1:c.7628A=	ENSP00000518343.1:p.Lys2543=
ENST00000649878.2:c.1577A=	ENSP00000497891.2:p.Lys526=
ENST00000685397.1:c.1577A=	ENSP00000509586.1:p.Lys526=
ENST00000686370.1:c.1577A=	ENSP00000509179.1:p.Lys526=
ENST00000689424.1:c.1835A=	ENSP00000509852.1:p.Lys612=
ENST00000691053.1:c.7610A=	ENSP00000509168.1:p.Lys2537=
ENST00000389506.10:c.7529A=	ENSP00000374157.5:p.Lys2510=
ENST00000528278.2:n.6880A=
ENST00000534358.8:c.7538A= MANE Select	ENSP00000436786.2:p.Lys2513=
ENST00000649699.1:c.7415A=	ENSP00000496927.1:p.Lys2472=
ENST00000389506.9:c.7529A=	ENSP00000374157.5:p.Lys2510=
ENST00000528278.1:n.1665A=
ENST00000534358.5:c.7538A=	ENSP00000436786.1:p.Lys2513=
NM_001197104.1:c.7538A= , LRG_613t1:c.7538A=	NP_001184033.1:p.Lys2513=
NM_005933.3:c.7529A=	NP_005924.2:p.Lys2510=
XM_006718839.2:c.5021A=	XP_006718902.2:p.Lys1674=
XM_011542829.1:c.7637A=	XP_011541131.1:p.Lys2546=
XM_011542830.1:c.7634A=	XP_011541132.1:p.Lys2545=
XM_011542831.1:c.7628A=	XP_011541133.1:p.Lys2543=
XM_011542832.1:c.5444A=	XP_011541134.1:p.Lys1815=
XM_011542833.1:c.5120A=	XP_011541135.1:p.Lys1707=
XM_006718839.3:c.5021A=	XP_006718902.2:p.Lys1674=
XM_011542829.2:c.7637A=	XP_011541131.1:p.Lys2546=
XM_011542830.2:c.7634A=	XP_011541132.1:p.Lys2545=
XM_011542831.2:c.7628A=	XP_011541133.1:p.Lys2543=
XM_011542833.2:c.5120A=	XP_011541135.1:p.Lys1707=
NM_001197104.2:c.7538A= MANE Select	NP_001184033.1:p.Lys2513=
NM_005933.4:c.7529A=	NP_005924.2:p.Lys2510=