Canonical Allele Identifier: CA2034964181

Gene: KMT2D

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49024858C= , CM000674.2:g.49024858C=	GRCh38
NC_000012.11:g.49418641C= , CM000674.1:g.49418641C=	GRCh37
NC_000012.10:g.47704908C=	NCBI36
NG_027827.1:g.35467G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681974.1:n.545G=
ENST00000683543.2:c.15873G=	ENSP00000506726.1:p.Glu5291=
ENST00000683863.1:n.1588G=
ENST00000684428.1:c.408G=	ENSP00000507433.1:p.Glu136=
ENST00000684755.1:n.408G=
ENST00000685024.1:c.998G=
ENST00000685166.1:c.15882G=	ENSP00000509386.1:p.Glu5294=
ENST00000688411.1:c.350G=	ENSP00000510146.1:n.350G=
ENST00000691463.1:c.1259G=	ENSP00000510624.1:n.1259G=
ENST00000692637.1:c.15870G=	ENSP00000509666.1:p.Glu5290=
ENST00000301067.12:c.15873G= MANE Select	ENSP00000301067.7:p.Glu5291=
ENST00000301067.11:c.15873G=	ENSP00000301067.7:p.Glu5291=
NM_003482.3:c.15873G=	NP_003473.3:p.Glu5291=
XM_005269162.3:c.15873G=	XP_005269219.1:p.Glu5291=
XM_006719614.2:c.15882G=	XP_006719677.1:p.Glu5294=
XM_006719616.2:c.15870G=	XP_006719679.1:p.Glu5290=
XM_011538770.1:c.15882G=	XP_011537072.1:p.Glu5294=
XM_011538771.1:c.15879G=	XP_011537073.1:p.Glu5293=
XM_011538772.1:c.15873G=	XP_011537074.1:p.Glu5291=
XM_011538773.1:c.15870G=	XP_011537075.1:p.Glu5290=
XM_011538774.1:c.15861G=	XP_011537076.1:p.Glu5287=
XM_011538775.1:c.15816G=	XP_011537077.1:p.Glu5272=
XM_011538776.1:c.15789G=	XP_011537078.1:p.Glu5263=
XR_944740.1:n.17061G=
XM_005269162.4:c.15873G=	XP_005269219.1:p.Glu5291=
XM_006719614.4:c.15882G=	XP_006719677.1:p.Glu5294=
XM_006719616.3:c.15870G=	XP_006719679.1:p.Glu5290=
XM_011538770.2:c.15882G=	XP_011537072.1:p.Glu5294=
XM_011538771.2:c.15879G=	XP_011537073.1:p.Glu5293=
XM_011538772.2:c.15873G=	XP_011537074.1:p.Glu5291=
XM_011538773.2:c.15870G=	XP_011537075.1:p.Glu5290=
XM_011538774.2:c.15861G=	XP_011537076.1:p.Glu5287=
XM_011538776.2:c.15789G=	XP_011537078.1:p.Glu5263=
XR_001748874.1:n.16050G=
NM_003482.4:c.15873G= MANE Select	NP_003473.3:p.Glu5291=