Canonical Allele Identifier: CA2034963289
Gene: KMT2D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49022598C= , CM000674.2:g.49022598C= GRCh38
NC_000012.11:g.49416381C= , CM000674.1:g.49416381C= GRCh37
NC_000012.10:g.47702648C= NCBI36
NG_027827.1:g.37727G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000526209.2:c.300G=
ENST00000681974.1:n.1002G=
ENST00000682693.1:n.1964G=
ENST00000682886.1:n.500G=
ENST00000683543.2:c.16378G= ENSP00000506726.1:p.Glu5460=
ENST00000683988.1:c.301G= ENSP00000506939.1:p.Glu101=
ENST00000684428.1:c.865G= ENSP00000507433.1:p.Glu289=
ENST00000684755.1:n.913G=
ENST00000685024.1:c.1484G=
ENST00000685166.1:c.16339G= ENSP00000509386.1:p.Glu5447=
ENST00000688411.1:c.807G= ENSP00000510146.1:n.807G=
ENST00000691932.1:c.331G= ENSP00000509037.1:p.Glu111=
ENST00000692637.1:c.16327G= ENSP00000509666.1:p.Glu5443=
ENST00000301067.12:c.16330G= MANE Select ENSP00000301067.7:p.Glu5444=
ENST00000301067.11:c.16330G= ENSP00000301067.7:p.Glu5444=
ENST00000526209.1:c.373G= ENSP00000435714.1:p.Glu125=
NM_003482.3:c.16330G= NP_003473.3:p.Glu5444=
XM_005269162.3:c.16330G= XP_005269219.1:p.Glu5444=
XM_006719614.2:c.16339G= XP_006719677.1:p.Glu5447=
XM_006719616.2:c.16327G= XP_006719679.1:p.Glu5443=
XM_011538770.1:c.16387G= XP_011537072.1:p.Glu5463=
XM_011538771.1:c.16384G= XP_011537073.1:p.Glu5462=
XM_011538772.1:c.16378G= XP_011537074.1:p.Glu5460=
XM_011538773.1:c.16375G= XP_011537075.1:p.Glu5459=
XM_011538774.1:c.16366G= XP_011537076.1:p.Glu5456=
XM_011538775.1:c.16321G= XP_011537077.1:p.Glu5441=
XM_011538776.1:c.16294G= XP_011537078.1:p.Glu5432=
XM_005269162.4:c.16330G= XP_005269219.1:p.Glu5444=
XM_006719614.4:c.16339G= XP_006719677.1:p.Glu5447=
XM_006719616.3:c.16327G= XP_006719679.1:p.Glu5443=
XM_011538770.2:c.16387G= XP_011537072.1:p.Glu5463=
XM_011538771.2:c.16384G= XP_011537073.1:p.Glu5462=
XM_011538772.2:c.16378G= XP_011537074.1:p.Glu5460=
XM_011538773.2:c.16375G= XP_011537075.1:p.Glu5459=
XM_011538774.2:c.16366G= XP_011537076.1:p.Glu5456=
XM_011538776.2:c.16294G= XP_011537078.1:p.Glu5432=
XR_001748874.1:n.16507G=
NM_003482.4:c.16330G= MANE Select NP_003473.3:p.Glu5444=