Canonical Allele Identifier: CA2034945918
Gene: KMT2D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49031719T= , CM000674.2:g.49031719T= GRCh38
NC_000012.11:g.49425502T= , CM000674.1:g.49425502T= GRCh37
NC_000012.10:g.47711769T= NCBI36
NG_027827.1:g.28606A=

Transcript Alleles

HGVS Amino-acid change
ENST00000683543.2:c.12986A= ENSP00000506726.1:p.Gln4329=
ENST00000685166.1:c.12995A= ENSP00000509386.1:p.Gln4332=
ENST00000685554.1:c.1753-407A= ENSP00000508640.1:n.1753-407A=
ENST00000692637.1:c.12983A= ENSP00000509666.1:p.Gln4328=
ENST00000692841.1:c.4465A= ENSP00000508711.1:n.4465A=
ENST00000301067.12:c.12986A= MANE Select ENSP00000301067.7:p.Gln4329=
ENST00000301067.11:c.12986A= ENSP00000301067.7:p.Gln4329=
NM_003482.3:c.12986A= NP_003473.3:p.Gln4329=
XM_005269162.3:c.12986A= XP_005269219.1:p.Gln4329=
XM_006719614.2:c.12995A= XP_006719677.1:p.Gln4332=
XM_006719616.2:c.12983A= XP_006719679.1:p.Gln4328=
XM_011538770.1:c.12995A= XP_011537072.1:p.Gln4332=
XM_011538771.1:c.12992A= XP_011537073.1:p.Gln4331=
XM_011538772.1:c.12986A= XP_011537074.1:p.Gln4329=
XM_011538773.1:c.12983A= XP_011537075.1:p.Gln4328=
XM_011538774.1:c.12974A= XP_011537076.1:p.Gln4325=
XM_011538775.1:c.12995A= XP_011537077.1:p.Gln4332=
XM_011538776.1:c.12902A= XP_011537078.1:p.Gln4301=
XR_944740.1:n.15315A=
XM_005269162.4:c.12986A= XP_005269219.1:p.Gln4329=
XM_006719614.4:c.12995A= XP_006719677.1:p.Gln4332=
XM_006719616.3:c.12983A= XP_006719679.1:p.Gln4328=
XM_011538770.2:c.12995A= XP_011537072.1:p.Gln4332=
XM_011538771.2:c.12992A= XP_011537073.1:p.Gln4331=
XM_011538772.2:c.12986A= XP_011537074.1:p.Gln4329=
XM_011538773.2:c.12983A= XP_011537075.1:p.Gln4328=
XM_011538774.2:c.12974A= XP_011537076.1:p.Gln4325=
XM_011538776.2:c.12902A= XP_011537078.1:p.Gln4301=
XR_001748874.1:n.14304A=
NM_003482.4:c.12986A= MANE Select NP_003473.3:p.Gln4329=