Canonical Allele Identifier: CA384682928
Gene: KMT2D HGNC NCBI

Linked Data

dbSNP Id: rs746132916

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49024868A>G , CM000674.2:g.49024868A>G GRCh38
NC_000012.11:g.49418651A>G , CM000674.1:g.49418651A>G GRCh37
NC_000012.10:g.47704918A>G NCBI36
NG_027827.1:g.35457T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000681974.1:n.535T>C
ENST00000683543.2:c.15863T>C ENSP00000506726.1:p.Leu5288Pro
ENST00000683863.1:n.1578T>C
ENST00000684428.1:c.398T>C ENSP00000507433.1:p.Leu133Pro
ENST00000684755.1:n.398T>C
ENST00000685024.1:c.988T>C
ENST00000685166.1:c.15872T>C ENSP00000509386.1:p.Leu5291Pro
ENST00000688411.1:c.340T>C ENSP00000510146.1:n.340T>C
ENST00000691463.1:c.1249T>C ENSP00000510624.1:n.1249T>C
ENST00000692637.1:c.15860T>C ENSP00000509666.1:p.Leu5287Pro
ENST00000301067.12:c.15863T>C MANE Select ENSP00000301067.7:p.Leu5288Pro
ENST00000301067.11:c.15863T>C ENSP00000301067.7:p.Leu5288Pro
NM_003482.3:c.15863T>C NP_003473.3:p.Leu5288Pro
XM_005269162.3:c.15863T>C XP_005269219.1:p.Leu5288Pro
XM_006719614.2:c.15872T>C XP_006719677.1:p.Leu5291Pro
XM_006719616.2:c.15860T>C XP_006719679.1:p.Leu5287Pro
XM_011538770.1:c.15872T>C XP_011537072.1:p.Leu5291Pro
XM_011538771.1:c.15869T>C XP_011537073.1:p.Leu5290Pro
XM_011538772.1:c.15863T>C XP_011537074.1:p.Leu5288Pro
XM_011538773.1:c.15860T>C XP_011537075.1:p.Leu5287Pro
XM_011538774.1:c.15851T>C XP_011537076.1:p.Leu5284Pro
XM_011538775.1:c.15806T>C XP_011537077.1:p.Leu5269Pro
XM_011538776.1:c.15779T>C XP_011537078.1:p.Leu5260Pro
XR_944740.1:n.17051T>C
XM_005269162.4:c.15863T>C XP_005269219.1:p.Leu5288Pro
XM_006719614.4:c.15872T>C XP_006719677.1:p.Leu5291Pro
XM_006719616.3:c.15860T>C XP_006719679.1:p.Leu5287Pro
XM_011538770.2:c.15872T>C XP_011537072.1:p.Leu5291Pro
XM_011538771.2:c.15869T>C XP_011537073.1:p.Leu5290Pro
XM_011538772.2:c.15863T>C XP_011537074.1:p.Leu5288Pro
XM_011538773.2:c.15860T>C XP_011537075.1:p.Leu5287Pro
XM_011538774.2:c.15851T>C XP_011537076.1:p.Leu5284Pro
XM_011538776.2:c.15779T>C XP_011537078.1:p.Leu5260Pro
XR_001748874.1:n.16040T>C
NM_003482.4:c.15863T>C MANE Select NP_003473.3:p.Leu5288Pro