Canonical Allele Identifier: CA384706852
Community Standard Title: NM_003482.4(KMT2D):c.13213C>T (p.Gln4405Ter)
Gene: KMT2D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49031492G>A , CM000674.2:g.49031492G>A GRCh38
NC_000012.11:g.49425275G>A , CM000674.1:g.49425275G>A GRCh37
NC_000012.10:g.47711542G>A NCBI36
NG_027827.1:g.28833C>T

Transcript Alleles

HGVS Amino-acid Change
NM_003482.4:c.13213C>T MANE Select NP_003473.3:p.Gln4405Ter
ENST00000301067.12:c.13213C>T MANE Select ENSP00000301067.7:p.Gln4405Ter
NM_003482.3:c.13213C>T NP_003473.3:p.Gln4405Ter
ENST00000301067.11:c.13213C>T ENSP00000301067.7:p.Gln4405Ter
ENST00000683543.2:c.13213C>T ENSP00000506726.1:p.Gln4405Ter
ENST00000685166.1:c.13222C>T ENSP00000509386.1:p.Gln4408Ter
ENST00000685554.1:c.1753-180C>T ENSP00000508640.1:n.1753-180C>T
ENST00000692637.1:c.13210C>T ENSP00000509666.1:p.Gln4404Ter
ENST00000692841.1:c.4692C>T ENSP00000508711.1:n.4692C>T
XM_005269162.3:c.13213C>T XP_005269219.1:p.Gln4405Ter
XM_005269162.4:c.13213C>T XP_005269219.1:p.Gln4405Ter
XM_006719614.2:c.13222C>T XP_006719677.1:p.Gln4408Ter
XM_006719614.4:c.13222C>T XP_006719677.1:p.Gln4408Ter
XM_006719616.2:c.13210C>T XP_006719679.1:p.Gln4404Ter
XM_006719616.3:c.13210C>T XP_006719679.1:p.Gln4404Ter
XM_011538770.1:c.13222C>T XP_011537072.1:p.Gln4408Ter
XM_011538770.2:c.13222C>T XP_011537072.1:p.Gln4408Ter
XM_011538771.1:c.13219C>T XP_011537073.1:p.Gln4407Ter
XM_011538771.2:c.13219C>T XP_011537073.1:p.Gln4407Ter
XM_011538772.1:c.13213C>T XP_011537074.1:p.Gln4405Ter
XM_011538772.2:c.13213C>T XP_011537074.1:p.Gln4405Ter
XM_011538773.1:c.13210C>T XP_011537075.1:p.Gln4404Ter
XM_011538773.2:c.13210C>T XP_011537075.1:p.Gln4404Ter
XM_011538774.1:c.13201C>T XP_011537076.1:p.Gln4401Ter
XM_011538774.2:c.13201C>T XP_011537076.1:p.Gln4401Ter
XM_011538775.1:c.13222C>T XP_011537077.1:p.Gln4408Ter
XM_011538776.1:c.13129C>T XP_011537078.1:p.Gln4377Ter
XM_011538776.2:c.13129C>T XP_011537078.1:p.Gln4377Ter
XR_001748874.1:n.14531C>T
XR_944740.1:n.15542C>T