Canonical Allele Identifier: CA384682874

Gene: KMT2D

Linked Data

• MyVariant Identifiers: chr12:g.49418643C>A (hg19) ; chr12:g.49024860C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49024860C>A , CM000674.2:g.49024860C>A	GRCh38
NC_000012.11:g.49418643C>A , CM000674.1:g.49418643C>A	GRCh37
NC_000012.10:g.47704910C>A	NCBI36
NG_027827.1:g.35465G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681974.1:n.543G>T
ENST00000683543.2:c.15871G>T	ENSP00000506726.1:p.Glu5291Ter
ENST00000683863.1:n.1586G>T
ENST00000684428.1:c.406G>T	ENSP00000507433.1:p.Glu136Ter
ENST00000684755.1:n.406G>T
ENST00000685024.1:c.996G>T
ENST00000685166.1:c.15880G>T	ENSP00000509386.1:p.Glu5294Ter
ENST00000688411.1:c.348G>T	ENSP00000510146.1:n.348G>T
ENST00000691463.1:c.1257G>T	ENSP00000510624.1:n.1257G>T
ENST00000692637.1:c.15868G>T	ENSP00000509666.1:p.Glu5290Ter
ENST00000301067.12:c.15871G>T MANE Select	ENSP00000301067.7:p.Glu5291Ter
ENST00000301067.11:c.15871G>T	ENSP00000301067.7:p.Glu5291Ter
NM_003482.3:c.15871G>T	NP_003473.3:p.Glu5291Ter
XM_005269162.3:c.15871G>T	XP_005269219.1:p.Glu5291Ter
XM_006719614.2:c.15880G>T	XP_006719677.1:p.Glu5294Ter
XM_006719616.2:c.15868G>T	XP_006719679.1:p.Glu5290Ter
XM_011538770.1:c.15880G>T	XP_011537072.1:p.Glu5294Ter
XM_011538771.1:c.15877G>T	XP_011537073.1:p.Glu5293Ter
XM_011538772.1:c.15871G>T	XP_011537074.1:p.Glu5291Ter
XM_011538773.1:c.15868G>T	XP_011537075.1:p.Glu5290Ter
XM_011538774.1:c.15859G>T	XP_011537076.1:p.Glu5287Ter
XM_011538775.1:c.15814G>T	XP_011537077.1:p.Glu5272Ter
XM_011538776.1:c.15787G>T	XP_011537078.1:p.Glu5263Ter
XR_944740.1:n.17059G>T
XM_005269162.4:c.15871G>T	XP_005269219.1:p.Glu5291Ter
XM_006719614.4:c.15880G>T	XP_006719677.1:p.Glu5294Ter
XM_006719616.3:c.15868G>T	XP_006719679.1:p.Glu5290Ter
XM_011538770.2:c.15880G>T	XP_011537072.1:p.Glu5294Ter
XM_011538771.2:c.15877G>T	XP_011537073.1:p.Glu5293Ter
XM_011538772.2:c.15871G>T	XP_011537074.1:p.Glu5291Ter
XM_011538773.2:c.15868G>T	XP_011537075.1:p.Glu5290Ter
XM_011538774.2:c.15859G>T	XP_011537076.1:p.Glu5287Ter
XM_011538776.2:c.15787G>T	XP_011537078.1:p.Glu5263Ter
XR_001748874.1:n.16048G>T
NM_003482.4:c.15871G>T MANE Select	NP_003473.3:p.Glu5291Ter