Canonical Allele Identifier: CA384649283
Gene: KMT2D HGNC NCBI

Linked Data

ClinVar Variation Id: 463015
ClinVar RCV Id: RCV000551228
dbSNP Id: rs1555195442

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49047997G>A , CM000674.2:g.49047997G>A GRCh38
NC_000012.11:g.49441780G>A , CM000674.1:g.49441780G>A GRCh37
NC_000012.10:g.47728047G>A NCBI36
NG_027827.1:g.12328C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000683543.2:c.4204C>T ENSP00000506726.1:p.Gln1402Ter
ENST00000685166.1:c.4204C>T ENSP00000509386.1:p.Gln1402Ter
ENST00000688095.1:c.184C>T ENSP00000510007.1:p.Gln62Ter
ENST00000692637.1:c.4201C>T ENSP00000509666.1:p.Gln1401Ter
ENST00000301067.12:c.4204C>T MANE Select ENSP00000301067.7:p.Gln1402Ter
ENST00000301067.11:c.4204C>T ENSP00000301067.7:p.Gln1402Ter
NM_003482.3:c.4204C>T NP_003473.3:p.Gln1402Ter
XM_005269162.3:c.4204C>T XP_005269219.1:p.Gln1402Ter
XM_006719614.2:c.4204C>T XP_006719677.1:p.Gln1402Ter
XM_006719616.2:c.4201C>T XP_006719679.1:p.Gln1401Ter
XM_011538770.1:c.4204C>T XP_011537072.1:p.Gln1402Ter
XM_011538771.1:c.4201C>T XP_011537073.1:p.Gln1401Ter
XM_011538772.1:c.4204C>T XP_011537074.1:p.Gln1402Ter
XM_011538773.1:c.4201C>T XP_011537075.1:p.Gln1401Ter
XM_011538774.1:c.4204C>T XP_011537076.1:p.Gln1402Ter
XM_011538775.1:c.4204C>T XP_011537077.1:p.Gln1402Ter
XM_011538776.1:c.4204C>T XP_011537078.1:p.Gln1402Ter
XR_944740.1:n.6524C>T
XM_005269162.4:c.4204C>T XP_005269219.1:p.Gln1402Ter
XM_006719614.4:c.4204C>T XP_006719677.1:p.Gln1402Ter
XM_006719616.3:c.4201C>T XP_006719679.1:p.Gln1401Ter
XM_011538770.2:c.4204C>T XP_011537072.1:p.Gln1402Ter
XM_011538771.2:c.4201C>T XP_011537073.1:p.Gln1401Ter
XM_011538772.2:c.4204C>T XP_011537074.1:p.Gln1402Ter
XM_011538773.2:c.4201C>T XP_011537075.1:p.Gln1401Ter
XM_011538774.2:c.4204C>T XP_011537076.1:p.Gln1402Ter
XM_011538776.2:c.4204C>T XP_011537078.1:p.Gln1402Ter
XR_001748874.1:n.5513C>T
NM_003482.4:c.4204C>T MANE Select NP_003473.3:p.Gln1402Ter