Canonical Allele Identifier: CA384682741

Gene: KMT2D

Linked Data

• MyVariant Identifiers: chr12:g.49418628G>T (hg19) ; chr12:g.49024845G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49024845G>T , CM000674.2:g.49024845G>T	GRCh38
NC_000012.11:g.49418628G>T , CM000674.1:g.49418628G>T	GRCh37
NC_000012.10:g.47704895G>T	NCBI36
NG_027827.1:g.35480C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681974.1:n.558C>A
ENST00000683543.2:c.15886C>A	ENSP00000506726.1:p.Leu5296Met
ENST00000683863.1:n.1601C>A
ENST00000684428.1:c.421C>A	ENSP00000507433.1:p.Leu141Met
ENST00000684755.1:n.421C>A
ENST00000685024.1:c.1011C>A
ENST00000685166.1:c.15895C>A	ENSP00000509386.1:p.Leu5299Met
ENST00000688411.1:c.363C>A	ENSP00000510146.1:n.363C>A
ENST00000691463.1:c.1272C>A	ENSP00000510624.1:n.1272C>A
ENST00000692637.1:c.15883C>A	ENSP00000509666.1:p.Leu5295Met
ENST00000301067.12:c.15886C>A MANE Select	ENSP00000301067.7:p.Leu5296Met
ENST00000301067.11:c.15886C>A	ENSP00000301067.7:p.Leu5296Met
NM_003482.3:c.15886C>A	NP_003473.3:p.Leu5296Met
XM_005269162.3:c.15886C>A	XP_005269219.1:p.Leu5296Met
XM_006719614.2:c.15895C>A	XP_006719677.1:p.Leu5299Met
XM_006719616.2:c.15883C>A	XP_006719679.1:p.Leu5295Met
XM_011538770.1:c.15895C>A	XP_011537072.1:p.Leu5299Met
XM_011538771.1:c.15892C>A	XP_011537073.1:p.Leu5298Met
XM_011538772.1:c.15886C>A	XP_011537074.1:p.Leu5296Met
XM_011538773.1:c.15883C>A	XP_011537075.1:p.Leu5295Met
XM_011538774.1:c.15874C>A	XP_011537076.1:p.Leu5292Met
XM_011538775.1:c.15829C>A	XP_011537077.1:p.Leu5277Met
XM_011538776.1:c.15802C>A	XP_011537078.1:p.Leu5268Met
XR_944740.1:n.17074C>A
XM_005269162.4:c.15886C>A	XP_005269219.1:p.Leu5296Met
XM_006719614.4:c.15895C>A	XP_006719677.1:p.Leu5299Met
XM_006719616.3:c.15883C>A	XP_006719679.1:p.Leu5295Met
XM_011538770.2:c.15895C>A	XP_011537072.1:p.Leu5299Met
XM_011538771.2:c.15892C>A	XP_011537073.1:p.Leu5298Met
XM_011538772.2:c.15886C>A	XP_011537074.1:p.Leu5296Met
XM_011538773.2:c.15883C>A	XP_011537075.1:p.Leu5295Met
XM_011538774.2:c.15874C>A	XP_011537076.1:p.Leu5292Met
XM_011538776.2:c.15802C>A	XP_011537078.1:p.Leu5268Met
XR_001748874.1:n.16063C>A
NM_003482.4:c.15886C>A MANE Select	NP_003473.3:p.Leu5296Met