Canonical Allele Identifier: CA2034963003
Gene: KMT2D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49022103T= , CM000674.2:g.49022103T= GRCh38
NC_000012.11:g.49415886T= , CM000674.1:g.49415886T= GRCh37
NC_000012.10:g.47702153T= NCBI36
NG_027827.1:g.38222A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000526209.2:c.431A=
ENST00000681974.1:n.1133A=
ENST00000682693.1:n.2095A=
ENST00000682886.1:n.867A=
ENST00000683543.2:c.16509A= ENSP00000506726.1:p.Thr5503=
ENST00000683988.1:c.432A= ENSP00000506939.1:p.Thr144=
ENST00000684428.1:c.1054A= ENSP00000507433.1:n.1054A=
ENST00000685024.1:c.1615A=
ENST00000685166.1:c.16470A= ENSP00000509386.1:p.Thr5490=
ENST00000691932.1:c.462A= ENSP00000509037.1:p.Thr154=
ENST00000692637.1:c.16458A= ENSP00000509666.1:p.Thr5486=
ENST00000301067.12:c.16461A= MANE Select ENSP00000301067.7:p.Thr5487=
ENST00000301067.11:c.16461A= ENSP00000301067.7:p.Thr5487=
ENST00000526209.1:c.504A= ENSP00000435714.1:p.Thr168=
NM_003482.3:c.16461A= NP_003473.3:p.Thr5487=
XM_005269162.3:c.16461A= XP_005269219.1:p.Thr5487=
XM_006719614.2:c.16470A= XP_006719677.1:p.Thr5490=
XM_006719616.2:c.16458A= XP_006719679.1:p.Thr5486=
XM_011538770.1:c.16518A= XP_011537072.1:p.Thr5506=
XM_011538771.1:c.16515A= XP_011537073.1:p.Thr5505=
XM_011538772.1:c.16509A= XP_011537074.1:p.Thr5503=
XM_011538773.1:c.16506A= XP_011537075.1:p.Thr5502=
XM_011538774.1:c.16497A= XP_011537076.1:p.Thr5499=
XM_011538775.1:c.16452A= XP_011537077.1:p.Thr5484=
XM_011538776.1:c.16425A= XP_011537078.1:p.Thr5475=
XM_005269162.4:c.16461A= XP_005269219.1:p.Thr5487=
XM_006719614.4:c.16470A= XP_006719677.1:p.Thr5490=
XM_006719616.3:c.16458A= XP_006719679.1:p.Thr5486=
XM_011538770.2:c.16518A= XP_011537072.1:p.Thr5506=
XM_011538771.2:c.16515A= XP_011537073.1:p.Thr5505=
XM_011538772.2:c.16509A= XP_011537074.1:p.Thr5503=
XM_011538773.2:c.16506A= XP_011537075.1:p.Thr5502=
XM_011538774.2:c.16497A= XP_011537076.1:p.Thr5499=
XM_011538776.2:c.16425A= XP_011537078.1:p.Thr5475=
XR_001748874.1:n.16638A=
NM_003482.4:c.16461A= MANE Select NP_003473.3:p.Thr5487=