Canonical Allele Identifier: CA384628187
Gene: KMT2D HGNC NCBI

Linked Data

dbSNP Id: rs2120557343

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49042601A>T , CM000674.2:g.49042601A>T GRCh38
NC_000012.11:g.49436384A>T , CM000674.1:g.49436384A>T GRCh37
NC_000012.10:g.47722651A>T NCBI36
NG_027827.1:g.17724T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650290.2:c.639T>A
ENST00000683543.2:c.5827T>A ENSP00000506726.1:p.Ser1943Thr
ENST00000685166.1:c.5836T>A ENSP00000509386.1:p.Ser1946Thr
ENST00000688095.1:c.1776T>A ENSP00000510007.1:n.1776T>A
ENST00000692637.1:c.5824T>A ENSP00000509666.1:p.Ser1942Thr
ENST00000301067.12:c.5827T>A MANE Select ENSP00000301067.7:p.Ser1943Thr
ENST00000301067.11:c.5827T>A ENSP00000301067.7:p.Ser1943Thr
NM_003482.3:c.5827T>A NP_003473.3:p.Ser1943Thr
XM_005269162.3:c.5827T>A XP_005269219.1:p.Ser1943Thr
XM_006719614.2:c.5836T>A XP_006719677.1:p.Ser1946Thr
XM_006719616.2:c.5824T>A XP_006719679.1:p.Ser1942Thr
XM_011538770.1:c.5836T>A XP_011537072.1:p.Ser1946Thr
XM_011538771.1:c.5833T>A XP_011537073.1:p.Ser1945Thr
XM_011538772.1:c.5827T>A XP_011537074.1:p.Ser1943Thr
XM_011538773.1:c.5824T>A XP_011537075.1:p.Ser1942Thr
XM_011538774.1:c.5836T>A XP_011537076.1:p.Ser1946Thr
XM_011538775.1:c.5836T>A XP_011537077.1:p.Ser1946Thr
XM_011538776.1:c.5836T>A XP_011537078.1:p.Ser1946Thr
XR_944740.1:n.8156T>A
XM_005269162.4:c.5827T>A XP_005269219.1:p.Ser1943Thr
XM_006719614.4:c.5836T>A XP_006719677.1:p.Ser1946Thr
XM_006719616.3:c.5824T>A XP_006719679.1:p.Ser1942Thr
XM_011538770.2:c.5836T>A XP_011537072.1:p.Ser1946Thr
XM_011538771.2:c.5833T>A XP_011537073.1:p.Ser1945Thr
XM_011538772.2:c.5827T>A XP_011537074.1:p.Ser1943Thr
XM_011538773.2:c.5824T>A XP_011537075.1:p.Ser1942Thr
XM_011538774.2:c.5836T>A XP_011537076.1:p.Ser1946Thr
XM_011538776.2:c.5836T>A XP_011537078.1:p.Ser1946Thr
XR_001748874.1:n.7145T>A
NM_003482.4:c.5827T>A MANE Select NP_003473.3:p.Ser1943Thr