Canonical Allele Identifier: CA2034947921

Gene: KMT2D

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49042205T= , CM000674.2:g.49042205T=	GRCh38
NC_000012.11:g.49435988T= , CM000674.1:g.49435988T=	GRCh37
NC_000012.10:g.47722255T=	NCBI36
NG_027827.1:g.18120A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650290.2:c.784A=
ENST00000683543.2:c.5993A=	ENSP00000506726.1:p.Tyr1998=
ENST00000685166.1:c.6002A=	ENSP00000509386.1:p.Tyr2001=
ENST00000689060.1:c.105A=
ENST00000689944.1:c.105A=
ENST00000692637.1:c.5990A=	ENSP00000509666.1:p.Tyr1997=
ENST00000301067.12:c.5993A= MANE Select	ENSP00000301067.7:p.Tyr1998=
ENST00000301067.11:c.5993A=	ENSP00000301067.7:p.Tyr1998=
NM_003482.3:c.5993A=	NP_003473.3:p.Tyr1998=
XM_005269162.3:c.5993A=	XP_005269219.1:p.Tyr1998=
XM_006719614.2:c.6002A=	XP_006719677.1:p.Tyr2001=
XM_006719616.2:c.5990A=	XP_006719679.1:p.Tyr1997=
XM_011538770.1:c.6002A=	XP_011537072.1:p.Tyr2001=
XM_011538771.1:c.5999A=	XP_011537073.1:p.Tyr2000=
XM_011538772.1:c.5993A=	XP_011537074.1:p.Tyr1998=
XM_011538773.1:c.5990A=	XP_011537075.1:p.Tyr1997=
XM_011538774.1:c.5981A=	XP_011537076.1:p.Tyr1994=
XM_011538775.1:c.6002A=	XP_011537077.1:p.Tyr2001=
XM_011538776.1:c.6002A=	XP_011537078.1:p.Tyr2001=
XR_944740.1:n.8322A=
XM_005269162.4:c.5993A=	XP_005269219.1:p.Tyr1998=
XM_006719614.4:c.6002A=	XP_006719677.1:p.Tyr2001=
XM_006719616.3:c.5990A=	XP_006719679.1:p.Tyr1997=
XM_011538770.2:c.6002A=	XP_011537072.1:p.Tyr2001=
XM_011538771.2:c.5999A=	XP_011537073.1:p.Tyr2000=
XM_011538772.2:c.5993A=	XP_011537074.1:p.Tyr1998=
XM_011538773.2:c.5990A=	XP_011537075.1:p.Tyr1997=
XM_011538774.2:c.5981A=	XP_011537076.1:p.Tyr1994=
XM_011538776.2:c.6002A=	XP_011537078.1:p.Tyr2001=
XR_001748874.1:n.7311A=
NM_003482.4:c.5993A= MANE Select	NP_003473.3:p.Tyr1998=