Canonical Allele Identifier: CA384683032

Gene: KMT2D

Linked Data

• dbSNP Id: rs2137711738
• MyVariant Identifiers: chr12:g.49418658C>G (hg19) ; chr12:g.49024875C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49024875C>G , CM000674.2:g.49024875C>G	GRCh38
NC_000012.11:g.49418658C>G , CM000674.1:g.49418658C>G	GRCh37
NC_000012.10:g.47704925C>G	NCBI36
NG_027827.1:g.35450G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681974.1:n.528G>C
ENST00000683543.2:c.15856G>C	ENSP00000506726.1:p.Glu5286Gln
ENST00000683863.1:n.1571G>C
ENST00000684428.1:c.391G>C	ENSP00000507433.1:p.Glu131Gln
ENST00000684755.1:n.391G>C
ENST00000685024.1:c.981G>C
ENST00000685166.1:c.15865G>C	ENSP00000509386.1:p.Glu5289Gln
ENST00000688411.1:c.333G>C	ENSP00000510146.1:n.333G>C
ENST00000691463.1:c.1242G>C	ENSP00000510624.1:n.1242G>C
ENST00000692637.1:c.15853G>C	ENSP00000509666.1:p.Glu5285Gln
ENST00000301067.12:c.15856G>C MANE Select	ENSP00000301067.7:p.Glu5286Gln
ENST00000301067.11:c.15856G>C	ENSP00000301067.7:p.Glu5286Gln
NM_003482.3:c.15856G>C	NP_003473.3:p.Glu5286Gln
XM_005269162.3:c.15856G>C	XP_005269219.1:p.Glu5286Gln
XM_006719614.2:c.15865G>C	XP_006719677.1:p.Glu5289Gln
XM_006719616.2:c.15853G>C	XP_006719679.1:p.Glu5285Gln
XM_011538770.1:c.15865G>C	XP_011537072.1:p.Glu5289Gln
XM_011538771.1:c.15862G>C	XP_011537073.1:p.Glu5288Gln
XM_011538772.1:c.15856G>C	XP_011537074.1:p.Glu5286Gln
XM_011538773.1:c.15853G>C	XP_011537075.1:p.Glu5285Gln
XM_011538774.1:c.15844G>C	XP_011537076.1:p.Glu5282Gln
XM_011538775.1:c.15799G>C	XP_011537077.1:p.Glu5267Gln
XM_011538776.1:c.15772G>C	XP_011537078.1:p.Glu5258Gln
XR_944740.1:n.17044G>C
XM_005269162.4:c.15856G>C	XP_005269219.1:p.Glu5286Gln
XM_006719614.4:c.15865G>C	XP_006719677.1:p.Glu5289Gln
XM_006719616.3:c.15853G>C	XP_006719679.1:p.Glu5285Gln
XM_011538770.2:c.15865G>C	XP_011537072.1:p.Glu5289Gln
XM_011538771.2:c.15862G>C	XP_011537073.1:p.Glu5288Gln
XM_011538772.2:c.15856G>C	XP_011537074.1:p.Glu5286Gln
XM_011538773.2:c.15853G>C	XP_011537075.1:p.Glu5285Gln
XM_011538774.2:c.15844G>C	XP_011537076.1:p.Glu5282Gln
XM_011538776.2:c.15772G>C	XP_011537078.1:p.Glu5258Gln
XR_001748874.1:n.16033G>C
NM_003482.4:c.15856G>C MANE Select	NP_003473.3:p.Glu5286Gln