Canonical Allele Identifier: CA2034963294
Gene: KMT2D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49022608C= , CM000674.2:g.49022608C= GRCh38
NC_000012.11:g.49416391C= , CM000674.1:g.49416391C= GRCh37
NC_000012.10:g.47702658C= NCBI36
NG_027827.1:g.37717G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000526209.2:c.290G=
ENST00000681974.1:n.992G=
ENST00000682693.1:n.1954G=
ENST00000682886.1:n.490G=
ENST00000683543.2:c.16368G= ENSP00000506726.1:p.Glu5456=
ENST00000683988.1:c.291G= ENSP00000506939.1:p.Glu97=
ENST00000684428.1:c.855G= ENSP00000507433.1:p.Glu285=
ENST00000684755.1:n.903G=
ENST00000685024.1:c.1474G=
ENST00000685166.1:c.16329G= ENSP00000509386.1:p.Glu5443=
ENST00000688411.1:c.797G= ENSP00000510146.1:n.797G=
ENST00000691932.1:c.321G= ENSP00000509037.1:p.Glu107=
ENST00000692637.1:c.16317G= ENSP00000509666.1:p.Glu5439=
ENST00000301067.12:c.16320G= MANE Select ENSP00000301067.7:p.Glu5440=
ENST00000301067.11:c.16320G= ENSP00000301067.7:p.Glu5440=
ENST00000526209.1:c.363G= ENSP00000435714.1:p.Glu121=
NM_003482.3:c.16320G= NP_003473.3:p.Glu5440=
XM_005269162.3:c.16320G= XP_005269219.1:p.Glu5440=
XM_006719614.2:c.16329G= XP_006719677.1:p.Glu5443=
XM_006719616.2:c.16317G= XP_006719679.1:p.Glu5439=
XM_011538770.1:c.16377G= XP_011537072.1:p.Glu5459=
XM_011538771.1:c.16374G= XP_011537073.1:p.Glu5458=
XM_011538772.1:c.16368G= XP_011537074.1:p.Glu5456=
XM_011538773.1:c.16365G= XP_011537075.1:p.Glu5455=
XM_011538774.1:c.16356G= XP_011537076.1:p.Glu5452=
XM_011538775.1:c.16311G= XP_011537077.1:p.Glu5437=
XM_011538776.1:c.16284G= XP_011537078.1:p.Glu5428=
XM_005269162.4:c.16320G= XP_005269219.1:p.Glu5440=
XM_006719614.4:c.16329G= XP_006719677.1:p.Glu5443=
XM_006719616.3:c.16317G= XP_006719679.1:p.Glu5439=
XM_011538770.2:c.16377G= XP_011537072.1:p.Glu5459=
XM_011538771.2:c.16374G= XP_011537073.1:p.Glu5458=
XM_011538772.2:c.16368G= XP_011537074.1:p.Glu5456=
XM_011538773.2:c.16365G= XP_011537075.1:p.Glu5455=
XM_011538774.2:c.16356G= XP_011537076.1:p.Glu5452=
XM_011538776.2:c.16284G= XP_011537078.1:p.Glu5428=
XR_001748874.1:n.16497G=
NM_003482.4:c.16320G= MANE Select NP_003473.3:p.Glu5440=