Canonical Allele Identifier: CA384682835

Gene: KMT2D

Linked Data

• dbSNP Id: rs2137711630
• MyVariant Identifiers: chr12:g.49418640C>G (hg19) ; chr12:g.49024857C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49024857C>G , CM000674.2:g.49024857C>G	GRCh38
NC_000012.11:g.49418640C>G , CM000674.1:g.49418640C>G	GRCh37
NC_000012.10:g.47704907C>G	NCBI36
NG_027827.1:g.35468G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681974.1:n.546G>C
ENST00000683543.2:c.15874G>C	ENSP00000506726.1:p.Glu5292Gln
ENST00000683863.1:n.1589G>C
ENST00000684428.1:c.409G>C	ENSP00000507433.1:p.Glu137Gln
ENST00000684755.1:n.409G>C
ENST00000685024.1:c.999G>C
ENST00000685166.1:c.15883G>C	ENSP00000509386.1:p.Glu5295Gln
ENST00000688411.1:c.351G>C	ENSP00000510146.1:n.351G>C
ENST00000691463.1:c.1260G>C	ENSP00000510624.1:n.1260G>C
ENST00000692637.1:c.15871G>C	ENSP00000509666.1:p.Glu5291Gln
ENST00000301067.12:c.15874G>C MANE Select	ENSP00000301067.7:p.Glu5292Gln
ENST00000301067.11:c.15874G>C	ENSP00000301067.7:p.Glu5292Gln
NM_003482.3:c.15874G>C	NP_003473.3:p.Glu5292Gln
XM_005269162.3:c.15874G>C	XP_005269219.1:p.Glu5292Gln
XM_006719614.2:c.15883G>C	XP_006719677.1:p.Glu5295Gln
XM_006719616.2:c.15871G>C	XP_006719679.1:p.Glu5291Gln
XM_011538770.1:c.15883G>C	XP_011537072.1:p.Glu5295Gln
XM_011538771.1:c.15880G>C	XP_011537073.1:p.Glu5294Gln
XM_011538772.1:c.15874G>C	XP_011537074.1:p.Glu5292Gln
XM_011538773.1:c.15871G>C	XP_011537075.1:p.Glu5291Gln
XM_011538774.1:c.15862G>C	XP_011537076.1:p.Glu5288Gln
XM_011538775.1:c.15817G>C	XP_011537077.1:p.Glu5273Gln
XM_011538776.1:c.15790G>C	XP_011537078.1:p.Glu5264Gln
XR_944740.1:n.17062G>C
XM_005269162.4:c.15874G>C	XP_005269219.1:p.Glu5292Gln
XM_006719614.4:c.15883G>C	XP_006719677.1:p.Glu5295Gln
XM_006719616.3:c.15871G>C	XP_006719679.1:p.Glu5291Gln
XM_011538770.2:c.15883G>C	XP_011537072.1:p.Glu5295Gln
XM_011538771.2:c.15880G>C	XP_011537073.1:p.Glu5294Gln
XM_011538772.2:c.15874G>C	XP_011537074.1:p.Glu5292Gln
XM_011538773.2:c.15871G>C	XP_011537075.1:p.Glu5291Gln
XM_011538774.2:c.15862G>C	XP_011537076.1:p.Glu5288Gln
XM_011538776.2:c.15790G>C	XP_011537078.1:p.Glu5264Gln
XR_001748874.1:n.16051G>C
NM_003482.4:c.15874G>C MANE Select	NP_003473.3:p.Glu5292Gln