Canonical Allele Identifier: CA2034947883

Gene: KMT2D

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49042179C= , CM000674.2:g.49042179C=	GRCh38
NC_000012.11:g.49435962C= , CM000674.1:g.49435962C=	GRCh37
NC_000012.10:g.47722229C=	NCBI36
NG_027827.1:g.18146G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650290.2:c.810G=
ENST00000683543.2:c.6019G=	ENSP00000506726.1:p.Glu2007=
ENST00000685166.1:c.6028G=	ENSP00000509386.1:p.Glu2010=
ENST00000689060.1:c.131G=
ENST00000689944.1:c.131G=
ENST00000692637.1:c.6016G=	ENSP00000509666.1:p.Glu2006=
ENST00000301067.12:c.6019G= MANE Select	ENSP00000301067.7:p.Glu2007=
ENST00000301067.11:c.6019G=	ENSP00000301067.7:p.Glu2007=
NM_003482.3:c.6019G=	NP_003473.3:p.Glu2007=
XM_005269162.3:c.6019G=	XP_005269219.1:p.Glu2007=
XM_006719614.2:c.6028G=	XP_006719677.1:p.Glu2010=
XM_006719616.2:c.6016G=	XP_006719679.1:p.Glu2006=
XM_011538770.1:c.6028G=	XP_011537072.1:p.Glu2010=
XM_011538771.1:c.6025G=	XP_011537073.1:p.Glu2009=
XM_011538772.1:c.6019G=	XP_011537074.1:p.Glu2007=
XM_011538773.1:c.6016G=	XP_011537075.1:p.Glu2006=
XM_011538774.1:c.6007G=	XP_011537076.1:p.Glu2003=
XM_011538775.1:c.6028G=	XP_011537077.1:p.Glu2010=
XM_011538776.1:c.6028G=	XP_011537078.1:p.Glu2010=
XR_944740.1:n.8348G=
XM_005269162.4:c.6019G=	XP_005269219.1:p.Glu2007=
XM_006719614.4:c.6028G=	XP_006719677.1:p.Glu2010=
XM_006719616.3:c.6016G=	XP_006719679.1:p.Glu2006=
XM_011538770.2:c.6028G=	XP_011537072.1:p.Glu2010=
XM_011538771.2:c.6025G=	XP_011537073.1:p.Glu2009=
XM_011538772.2:c.6019G=	XP_011537074.1:p.Glu2007=
XM_011538773.2:c.6016G=	XP_011537075.1:p.Glu2006=
XM_011538774.2:c.6007G=	XP_011537076.1:p.Glu2003=
XM_011538776.2:c.6028G=	XP_011537078.1:p.Glu2010=
XR_001748874.1:n.7337G=
NM_003482.4:c.6019G= MANE Select	NP_003473.3:p.Glu2007=