Canonical Allele Identifier: CA2695216443

Gene: KMT2D

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49042174del , CM000674.2:g.49042174del	GRCh38
NC_000012.11:g.49435957del , CM000674.1:g.49435957del	GRCh37
NC_000012.10:g.47722224del	NCBI36
NG_027827.1:g.18152del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650290.2:c.816del
ENST00000683543.2:c.6025del	ENSP00000506726.1:p.Asp2009MetfsTer?
ENST00000685166.1:c.6034del	ENSP00000509386.1:p.Asp2012MetfsTer?
ENST00000689060.1:c.137del
ENST00000689944.1:c.137del
ENST00000692637.1:c.6022del	ENSP00000509666.1:p.Asp2008MetfsTer?
ENST00000301067.12:c.6025del MANE Select	ENSP00000301067.7:p.Asp2009MetfsTer?
ENST00000301067.11:c.6025del	ENSP00000301067.7:p.Asp2009MetfsTer?
NM_003482.3:c.6025del	NP_003473.3:p.Asp2009MetfsTer?
XM_005269162.3:c.6025del	XP_005269219.1:p.Asp2009MetfsTer?
XM_006719614.2:c.6034del	XP_006719677.1:p.Asp2012MetfsTer?
XM_006719616.2:c.6022del	XP_006719679.1:p.Asp2008MetfsTer?
XM_011538770.1:c.6034del	XP_011537072.1:p.Asp2012MetfsTer?
XM_011538771.1:c.6031del	XP_011537073.1:p.Asp2011MetfsTer?
XM_011538772.1:c.6025del	XP_011537074.1:p.Asp2009MetfsTer?
XM_011538773.1:c.6022del	XP_011537075.1:p.Asp2008MetfsTer?
XM_011538774.1:c.6013del	XP_011537076.1:p.Asp2005MetfsTer?
XM_011538775.1:c.6034del	XP_011537077.1:p.Asp2012MetfsTer?
XM_011538776.1:c.6034del	XP_011537078.1:p.Asp2012MetfsTer?
XR_944740.1:n.8354del
XM_005269162.4:c.6025del	XP_005269219.1:p.Asp2009MetfsTer?
XM_006719614.4:c.6034del	XP_006719677.1:p.Asp2012MetfsTer?
XM_006719616.3:c.6022del	XP_006719679.1:p.Asp2008MetfsTer?
XM_011538770.2:c.6034del	XP_011537072.1:p.Asp2012MetfsTer?
XM_011538771.2:c.6031del	XP_011537073.1:p.Asp2011MetfsTer?
XM_011538772.2:c.6025del	XP_011537074.1:p.Asp2009MetfsTer?
XM_011538773.2:c.6022del	XP_011537075.1:p.Asp2008MetfsTer?
XM_011538774.2:c.6013del	XP_011537076.1:p.Asp2005MetfsTer?
XM_011538776.2:c.6034del	XP_011537078.1:p.Asp2012MetfsTer?
XR_001748874.1:n.7343del
NM_003482.4:c.6025del MANE Select	NP_003473.3:p.Asp2009MetfsTer?