Canonical Allele Identifier: CA236639171
Gene: KMT2D HGNC NCBI

Linked Data

dbSNP Id: rs1018226370

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49031923G>C , CM000674.2:g.49031923G>C GRCh38
NC_000012.11:g.49425706G>C , CM000674.1:g.49425706G>C GRCh37
NC_000012.10:g.47711973G>C NCBI36
NG_027827.1:g.28402C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000683543.2:c.12782C>G ENSP00000506726.1:p.Pro4261Arg
ENST00000685166.1:c.12791C>G ENSP00000509386.1:p.Pro4264Arg
ENST00000685554.1:c.1752+590C>G ENSP00000508640.1:n.1752+590C>G
ENST00000692637.1:c.12779C>G ENSP00000509666.1:p.Pro4260Arg
ENST00000692841.1:c.4261C>G ENSP00000508711.1:n.4261C>G
ENST00000301067.12:c.12782C>G MANE Select ENSP00000301067.7:p.Pro4261Arg
ENST00000301067.11:c.12782C>G ENSP00000301067.7:p.Pro4261Arg
NM_003482.3:c.12782C>G NP_003473.3:p.Pro4261Arg
XM_005269162.3:c.12782C>G XP_005269219.1:p.Pro4261Arg
XM_006719614.2:c.12791C>G XP_006719677.1:p.Pro4264Arg
XM_006719616.2:c.12779C>G XP_006719679.1:p.Pro4260Arg
XM_011538770.1:c.12791C>G XP_011537072.1:p.Pro4264Arg
XM_011538771.1:c.12788C>G XP_011537073.1:p.Pro4263Arg
XM_011538772.1:c.12782C>G XP_011537074.1:p.Pro4261Arg
XM_011538773.1:c.12779C>G XP_011537075.1:p.Pro4260Arg
XM_011538774.1:c.12770C>G XP_011537076.1:p.Pro4257Arg
XM_011538775.1:c.12791C>G XP_011537077.1:p.Pro4264Arg
XM_011538776.1:c.12698C>G XP_011537078.1:p.Pro4233Arg
XR_944740.1:n.15111C>G
XM_005269162.4:c.12782C>G XP_005269219.1:p.Pro4261Arg
XM_006719614.4:c.12791C>G XP_006719677.1:p.Pro4264Arg
XM_006719616.3:c.12779C>G XP_006719679.1:p.Pro4260Arg
XM_011538770.2:c.12791C>G XP_011537072.1:p.Pro4264Arg
XM_011538771.2:c.12788C>G XP_011537073.1:p.Pro4263Arg
XM_011538772.2:c.12782C>G XP_011537074.1:p.Pro4261Arg
XM_011538773.2:c.12779C>G XP_011537075.1:p.Pro4260Arg
XM_011538774.2:c.12770C>G XP_011537076.1:p.Pro4257Arg
XM_011538776.2:c.12698C>G XP_011537078.1:p.Pro4233Arg
XR_001748874.1:n.14100C>G
NM_003482.4:c.12782C>G MANE Select NP_003473.3:p.Pro4261Arg