Canonical Allele Identifier: CA2034964018

Gene: KMT2D

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49024455_49024457delinsAAG , CM000674.2:g.49024455_49024457delinsAAG	GRCh38
NC_000012.11:g.49418238_49418240delinsAAG , CM000674.1:g.49418238_49418240delinsAAG	GRCh37
NC_000012.10:g.47704505_47704507delinsAAG	NCBI36
NG_027827.1:g.35868_35870delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681974.1:n.724+121_724+123delinsCTT
ENST00000682693.1:n.105_107delinsCTT
ENST00000683543.2:c.16052+121_16052+123delinsCTT	ENSP00000506726.1:n.16052+121_16052+123delinsCTT
ENST00000683863.1:n.1888_1890delinsCTT
ENST00000684428.1:c.587+121_587+123delinsCTT	ENSP00000507433.1:n.587+121_587+123delinsCTT
ENST00000684755.1:n.587+121_587+123delinsCTT
ENST00000685024.1:c.1206+121_1206+123delinsCTT
ENST00000685166.1:c.16061+121_16061+123delinsCTT	ENSP00000509386.1:n.16061+121_16061+123delinsCTT
ENST00000688411.1:c.529+121_529+123delinsCTT	ENSP00000510146.1:n.529+121_529+123delinsCTT
ENST00000691932.1:c.131+121_131+123delinsCTT	ENSP00000509037.1:n.131+121_131+123delinsCTT
ENST00000692637.1:c.16049+121_16049+123delinsCTT	ENSP00000509666.1:n.16049+121_16049+123delinsCTT
ENST00000301067.12:c.16052+121_16052+123delinsCTT MANE Select	ENSP00000301067.7:n.16052+121_16052+123delinsCTT
ENST00000301067.11:c.16052+121_16052+123delinsCTT	ENSP00000301067.7:n.16052+121_16052+123delinsCTT
ENST00000526209.1:c.47+121_47+123delinsCTT	ENSP00000435714.1:n.47+121_47+123delinsCTT
NM_003482.3:c.16052+121_16052+123delinsCTT	NP_003473.3:n.16052+121_16052+123delinsCTT
XM_005269162.3:c.16052+121_16052+123delinsCTT	XP_005269219.1:n.16052+121_16052+123delinsCTT
XM_006719614.2:c.16061+121_16061+123delinsCTT	XP_006719677.1:n.16061+121_16061+123delinsCTT
XM_006719616.2:c.16049+121_16049+123delinsCTT	XP_006719679.1:n.16049+121_16049+123delinsCTT
XM_011538770.1:c.16061+121_16061+123delinsCTT	XP_011537072.1:n.16061+121_16061+123delinsCTT
XM_011538771.1:c.16058+121_16058+123delinsCTT	XP_011537073.1:n.16058+121_16058+123delinsCTT
XM_011538772.1:c.16052+121_16052+123delinsCTT	XP_011537074.1:n.16052+121_16052+123delinsCTT
XM_011538773.1:c.16049+121_16049+123delinsCTT	XP_011537075.1:n.16049+121_16049+123delinsCTT
XM_011538774.1:c.16040+121_16040+123delinsCTT	XP_011537076.1:n.16040+121_16040+123delinsCTT
XM_011538775.1:c.15995+121_15995+123delinsCTT	XP_011537077.1:n.15995+121_15995+123delinsCTT
XM_011538776.1:c.15968+121_15968+123delinsCTT	XP_011537078.1:n.15968+121_15968+123delinsCTT
XM_005269162.4:c.16052+121_16052+123delinsCTT	XP_005269219.1:n.16052+121_16052+123delinsCTT
XM_006719614.4:c.16061+121_16061+123delinsCTT	XP_006719677.1:n.16061+121_16061+123delinsCTT
XM_006719616.3:c.16049+121_16049+123delinsCTT	XP_006719679.1:n.16049+121_16049+123delinsCTT
XM_011538770.2:c.16061+121_16061+123delinsCTT	XP_011537072.1:n.16061+121_16061+123delinsCTT
XM_011538771.2:c.16058+121_16058+123delinsCTT	XP_011537073.1:n.16058+121_16058+123delinsCTT
XM_011538772.2:c.16052+121_16052+123delinsCTT	XP_011537074.1:n.16052+121_16052+123delinsCTT
XM_011538773.2:c.16049+121_16049+123delinsCTT	XP_011537075.1:n.16049+121_16049+123delinsCTT
XM_011538774.2:c.16040+121_16040+123delinsCTT	XP_011537076.1:n.16040+121_16040+123delinsCTT
XM_011538776.2:c.15968+121_15968+123delinsCTT	XP_011537078.1:n.15968+121_15968+123delinsCTT
XR_001748874.1:n.16229+121_16229+123delinsCTT
NM_003482.4:c.16052+121_16052+123delinsCTT MANE Select	NP_003473.3:n.16052+121_16052+123delinsCTT