Canonical Allele Identifier: CA6546818

Gene: KMT2D

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49038777C>T , CM000674.2:g.49038777C>T	GRCh38
NC_000012.11:g.49432560C>T , CM000674.1:g.49432560C>T	GRCh37
NC_000012.10:g.47718827C>T	NCBI36
NG_027827.1:g.21548G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003482.4:c.8579G>A MANE Select	NP_003473.3:p.Arg2860His
ENST00000301067.12:c.8579G>A MANE Select	ENSP00000301067.7:p.Arg2860His
NM_003482.3:c.8579G>A	NP_003473.3:p.Arg2860His
ENST00000301067.11:c.8579G>A	ENSP00000301067.7:p.Arg2860His
ENST00000549799.1:n.221G>A
ENST00000683043.1:n.278G>A
ENST00000683543.2:c.8579G>A	ENSP00000506726.1:p.Arg2860His
ENST00000685166.1:c.8588G>A	ENSP00000509386.1:p.Arg2863His
ENST00000687201.1:c.143G>A	ENSP00000510037.1:p.Arg48His
ENST00000689143.1:c.2182G>A	ENSP00000509839.1:n.2182G>A
ENST00000692637.1:c.8576G>A	ENSP00000509666.1:p.Arg2859His
ENST00000692841.1:c.143G>A	ENSP00000508711.1:p.Arg48His
XM_005269162.3:c.8579G>A	XP_005269219.1:p.Arg2860His
XM_005269162.4:c.8579G>A	XP_005269219.1:p.Arg2860His
XM_006719614.2:c.8588G>A	XP_006719677.1:p.Arg2863His
XM_006719614.4:c.8588G>A	XP_006719677.1:p.Arg2863His
XM_006719616.2:c.8576G>A	XP_006719679.1:p.Arg2859His
XM_006719616.3:c.8576G>A	XP_006719679.1:p.Arg2859His
XM_011538770.1:c.8588G>A	XP_011537072.1:p.Arg2863His
XM_011538770.2:c.8588G>A	XP_011537072.1:p.Arg2863His
XM_011538771.1:c.8585G>A	XP_011537073.1:p.Arg2862His
XM_011538771.2:c.8585G>A	XP_011537073.1:p.Arg2862His
XM_011538772.1:c.8579G>A	XP_011537074.1:p.Arg2860His
XM_011538772.2:c.8579G>A	XP_011537074.1:p.Arg2860His
XM_011538773.1:c.8576G>A	XP_011537075.1:p.Arg2859His
XM_011538773.2:c.8576G>A	XP_011537075.1:p.Arg2859His
XM_011538774.1:c.8567G>A	XP_011537076.1:p.Arg2856His
XM_011538774.2:c.8567G>A	XP_011537076.1:p.Arg2856His
XM_011538775.1:c.8588G>A	XP_011537077.1:p.Arg2863His
XM_011538776.1:c.8495G>A	XP_011537078.1:p.Arg2832His
XM_011538776.2:c.8495G>A	XP_011537078.1:p.Arg2832His
XR_001748874.1:n.9897G>A
XR_944740.1:n.10908G>A