Canonical Allele Identifier: CA384717193
Gene: KMT2D HGNC NCBI

Linked Data

dbSNP Id: rs1565777725

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49033102C>A , CM000674.2:g.49033102C>A GRCh38
NC_000012.11:g.49426885C>A , CM000674.1:g.49426885C>A GRCh37
NC_000012.10:g.47713152C>A NCBI36
NG_027827.1:g.27223G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000683543.2:c.11603G>T ENSP00000506726.1:p.Gly3868Val
ENST00000685166.1:c.11612G>T ENSP00000509386.1:p.Gly3871Val
ENST00000685554.1:c.1163G>T ENSP00000508640.1:p.Gly388Val
ENST00000687201.1:c.3182G>T ENSP00000510037.1:p.Gly1061Val
ENST00000692637.1:c.11600G>T ENSP00000509666.1:p.Gly3867Val
ENST00000692841.1:c.3082G>T ENSP00000508711.1:n.3082G>T
ENST00000301067.12:c.11603G>T MANE Select ENSP00000301067.7:p.Gly3868Val
ENST00000301067.11:c.11603G>T ENSP00000301067.7:p.Gly3868Val
NM_003482.3:c.11603G>T NP_003473.3:p.Gly3868Val
XM_005269162.3:c.11603G>T XP_005269219.1:p.Gly3868Val
XM_006719614.2:c.11612G>T XP_006719677.1:p.Gly3871Val
XM_006719616.2:c.11600G>T XP_006719679.1:p.Gly3867Val
XM_011538770.1:c.11612G>T XP_011537072.1:p.Gly3871Val
XM_011538771.1:c.11609G>T XP_011537073.1:p.Gly3870Val
XM_011538772.1:c.11603G>T XP_011537074.1:p.Gly3868Val
XM_011538773.1:c.11600G>T XP_011537075.1:p.Gly3867Val
XM_011538774.1:c.11591G>T XP_011537076.1:p.Gly3864Val
XM_011538775.1:c.11612G>T XP_011537077.1:p.Gly3871Val
XM_011538776.1:c.11519G>T XP_011537078.1:p.Gly3840Val
XR_944740.1:n.13932G>T
XM_005269162.4:c.11603G>T XP_005269219.1:p.Gly3868Val
XM_006719614.4:c.11612G>T XP_006719677.1:p.Gly3871Val
XM_006719616.3:c.11600G>T XP_006719679.1:p.Gly3867Val
XM_011538770.2:c.11612G>T XP_011537072.1:p.Gly3871Val
XM_011538771.2:c.11609G>T XP_011537073.1:p.Gly3870Val
XM_011538772.2:c.11603G>T XP_011537074.1:p.Gly3868Val
XM_011538773.2:c.11600G>T XP_011537075.1:p.Gly3867Val
XM_011538774.2:c.11591G>T XP_011537076.1:p.Gly3864Val
XM_011538776.2:c.11519G>T XP_011537078.1:p.Gly3840Val
XR_001748874.1:n.12921G>T
NM_003482.4:c.11603G>T MANE Select NP_003473.3:p.Gly3868Val