Canonical Allele Identifier: CA384683006

Gene: KMT2D

Linked Data

• dbSNP Id: rs770257093
• MyVariant Identifiers: chr12:g.49418656C>G (hg19) ; chr12:g.49024873C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49024873C>G , CM000674.2:g.49024873C>G	GRCh38
NC_000012.11:g.49418656C>G , CM000674.1:g.49418656C>G	GRCh37
NC_000012.10:g.47704923C>G	NCBI36
NG_027827.1:g.35452G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681974.1:n.530G>C
ENST00000683543.2:c.15858G>C	ENSP00000506726.1:p.Glu5286Asp
ENST00000683863.1:n.1573G>C
ENST00000684428.1:c.393G>C	ENSP00000507433.1:p.Glu131Asp
ENST00000684755.1:n.393G>C
ENST00000685024.1:c.983G>C
ENST00000685166.1:c.15867G>C	ENSP00000509386.1:p.Glu5289Asp
ENST00000688411.1:c.335G>C	ENSP00000510146.1:n.335G>C
ENST00000691463.1:c.1244G>C	ENSP00000510624.1:n.1244G>C
ENST00000692637.1:c.15855G>C	ENSP00000509666.1:p.Glu5285Asp
ENST00000301067.12:c.15858G>C MANE Select	ENSP00000301067.7:p.Glu5286Asp
ENST00000301067.11:c.15858G>C	ENSP00000301067.7:p.Glu5286Asp
NM_003482.3:c.15858G>C	NP_003473.3:p.Glu5286Asp
XM_005269162.3:c.15858G>C	XP_005269219.1:p.Glu5286Asp
XM_006719614.2:c.15867G>C	XP_006719677.1:p.Glu5289Asp
XM_006719616.2:c.15855G>C	XP_006719679.1:p.Glu5285Asp
XM_011538770.1:c.15867G>C	XP_011537072.1:p.Glu5289Asp
XM_011538771.1:c.15864G>C	XP_011537073.1:p.Glu5288Asp
XM_011538772.1:c.15858G>C	XP_011537074.1:p.Glu5286Asp
XM_011538773.1:c.15855G>C	XP_011537075.1:p.Glu5285Asp
XM_011538774.1:c.15846G>C	XP_011537076.1:p.Glu5282Asp
XM_011538775.1:c.15801G>C	XP_011537077.1:p.Glu5267Asp
XM_011538776.1:c.15774G>C	XP_011537078.1:p.Glu5258Asp
XR_944740.1:n.17046G>C
XM_005269162.4:c.15858G>C	XP_005269219.1:p.Glu5286Asp
XM_006719614.4:c.15867G>C	XP_006719677.1:p.Glu5289Asp
XM_006719616.3:c.15855G>C	XP_006719679.1:p.Glu5285Asp
XM_011538770.2:c.15867G>C	XP_011537072.1:p.Glu5289Asp
XM_011538771.2:c.15864G>C	XP_011537073.1:p.Glu5288Asp
XM_011538772.2:c.15858G>C	XP_011537074.1:p.Glu5286Asp
XM_011538773.2:c.15855G>C	XP_011537075.1:p.Glu5285Asp
XM_011538774.2:c.15846G>C	XP_011537076.1:p.Glu5282Asp
XM_011538776.2:c.15774G>C	XP_011537078.1:p.Glu5258Asp
XR_001748874.1:n.16035G>C
NM_003482.4:c.15858G>C MANE Select	NP_003473.3:p.Glu5286Asp