Canonical Allele Identifier: CA6545806

Gene: KMT2D

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49029108C>T , CM000674.2:g.49029108C>T	GRCh38
NC_000012.11:g.49422891C>T , CM000674.1:g.49422891C>T	GRCh37
NC_000012.10:g.47709158C>T	NCBI36
NG_027827.1:g.31217G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003482.4:c.14204G>A MANE Select	NP_003473.3:p.Arg4735Gln
ENST00000301067.12:c.14204G>A MANE Select	ENSP00000301067.7:p.Arg4735Gln
NM_003482.3:c.14204G>A	NP_003473.3:p.Arg4735Gln
ENST00000301067.11:c.14204G>A	ENSP00000301067.7:p.Arg4735Gln
ENST00000683543.2:c.14204G>A	ENSP00000506726.1:p.Arg4735Gln
ENST00000685166.1:c.14213G>A	ENSP00000509386.1:p.Arg4738Gln
ENST00000685979.1:c.467G>A	ENSP00000508906.1:p.Arg156Gln
ENST00000686564.1:c.464G>A	ENSP00000509290.1:p.Arg155Gln
ENST00000687241.1:c.296G>A	ENSP00000509842.1:p.Arg99Gln
ENST00000691986.1:c.503G>A	ENSP00000509196.1:p.Arg168Gln
ENST00000692637.1:c.14201G>A	ENSP00000509666.1:p.Arg4734Gln
XM_005269162.3:c.14204G>A	XP_005269219.1:p.Arg4735Gln
XM_005269162.4:c.14204G>A	XP_005269219.1:p.Arg4735Gln
XM_006719614.2:c.14213G>A	XP_006719677.1:p.Arg4738Gln
XM_006719614.4:c.14213G>A	XP_006719677.1:p.Arg4738Gln
XM_006719616.2:c.14201G>A	XP_006719679.1:p.Arg4734Gln
XM_006719616.3:c.14201G>A	XP_006719679.1:p.Arg4734Gln
XM_011538770.1:c.14213G>A	XP_011537072.1:p.Arg4738Gln
XM_011538770.2:c.14213G>A	XP_011537072.1:p.Arg4738Gln
XM_011538771.1:c.14210G>A	XP_011537073.1:p.Arg4737Gln
XM_011538771.2:c.14210G>A	XP_011537073.1:p.Arg4737Gln
XM_011538772.1:c.14204G>A	XP_011537074.1:p.Arg4735Gln
XM_011538772.2:c.14204G>A	XP_011537074.1:p.Arg4735Gln
XM_011538773.1:c.14201G>A	XP_011537075.1:p.Arg4734Gln
XM_011538773.2:c.14201G>A	XP_011537075.1:p.Arg4734Gln
XM_011538774.1:c.14192G>A	XP_011537076.1:p.Arg4731Gln
XM_011538774.2:c.14192G>A	XP_011537076.1:p.Arg4731Gln
XM_011538775.1:c.14147G>A	XP_011537077.1:p.Arg4716Gln
XM_011538776.1:c.14120G>A	XP_011537078.1:p.Arg4707Gln
XM_011538776.2:c.14120G>A	XP_011537078.1:p.Arg4707Gln
XR_001748874.1:n.15522G>A
XR_944740.1:n.16533G>A