Canonical Allele Identifier: CA2034958931

Gene: KMT2D

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49039164A= , CM000674.2:g.49039164A=	GRCh38
NC_000012.11:g.49432947A= , CM000674.1:g.49432947A=	GRCh37
NC_000012.10:g.47719214A=	NCBI36
NG_027827.1:g.21161T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683043.1:n.65+58T=
ENST00000683543.2:c.8366+58T=	ENSP00000506726.1:n.8366+58T=
ENST00000685166.1:c.8375+58T=	ENSP00000509386.1:n.8375+58T=
ENST00000689143.1:c.2039+58T=	ENSP00000509839.1:n.2039+58T=
ENST00000692637.1:c.8363+58T=	ENSP00000509666.1:n.8363+58T=
ENST00000301067.12:c.8366+58T= MANE Select	ENSP00000301067.7:n.8366+58T=
ENST00000301067.11:c.8366+58T=	ENSP00000301067.7:n.8366+58T=
ENST00000549799.1:n.78+58T=
NM_003482.3:c.8366+58T=	NP_003473.3:n.8366+58T=
XM_005269162.3:c.8366+58T=	XP_005269219.1:n.8366+58T=
XM_006719614.2:c.8375+58T=	XP_006719677.1:n.8375+58T=
XM_006719616.2:c.8363+58T=	XP_006719679.1:n.8363+58T=
XM_011538770.1:c.8375+58T=	XP_011537072.1:n.8375+58T=
XM_011538771.1:c.8372+58T=	XP_011537073.1:n.8372+58T=
XM_011538772.1:c.8366+58T=	XP_011537074.1:n.8366+58T=
XM_011538773.1:c.8363+58T=	XP_011537075.1:n.8363+58T=
XM_011538774.1:c.8354+58T=	XP_011537076.1:n.8354+58T=
XM_011538775.1:c.8375+58T=	XP_011537077.1:n.8375+58T=
XM_011538776.1:c.8282+58T=	XP_011537078.1:n.8282+58T=
XR_944740.1:n.10695+58T=
XM_005269162.4:c.8366+58T=	XP_005269219.1:n.8366+58T=
XM_006719614.4:c.8375+58T=	XP_006719677.1:n.8375+58T=
XM_006719616.3:c.8363+58T=	XP_006719679.1:n.8363+58T=
XM_011538770.2:c.8375+58T=	XP_011537072.1:n.8375+58T=
XM_011538771.2:c.8372+58T=	XP_011537073.1:n.8372+58T=
XM_011538772.2:c.8366+58T=	XP_011537074.1:n.8366+58T=
XM_011538773.2:c.8363+58T=	XP_011537075.1:n.8363+58T=
XM_011538774.2:c.8354+58T=	XP_011537076.1:n.8354+58T=
XM_011538776.2:c.8282+58T=	XP_011537078.1:n.8282+58T=
XR_001748874.1:n.9684+58T=
NM_003482.4:c.8366+58T= MANE Select	NP_003473.3:n.8366+58T=