Canonical Allele Identifier: CA6546871
Gene: KMT2D HGNC NCBI

Linked Data

dbSNP Id: rs369611929

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49039284G>C , CM000674.2:g.49039284G>C GRCh38
NC_000012.11:g.49433067G>C , CM000674.1:g.49433067G>C GRCh37
NC_000012.10:g.47719334G>C NCBI36
NG_027827.1:g.21041C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000683043.1:n.3C>G
ENST00000683543.2:c.8304C>G ENSP00000506726.1:p.Ser2768Arg
ENST00000685166.1:c.8313C>G ENSP00000509386.1:p.Ser2771Arg
ENST00000689060.1:c.2323C>G
ENST00000689143.1:c.1977C>G ENSP00000509839.1:p.Ser659Arg
ENST00000689944.1:c.2413C>G
ENST00000692637.1:c.8301C>G ENSP00000509666.1:p.Ser2767Arg
ENST00000301067.12:c.8304C>G MANE Select ENSP00000301067.7:p.Ser2768Arg
ENST00000301067.11:c.8304C>G ENSP00000301067.7:p.Ser2768Arg
ENST00000549799.1:n.16C>G
NM_003482.3:c.8304C>G NP_003473.3:p.Ser2768Arg
XM_005269162.3:c.8304C>G XP_005269219.1:p.Ser2768Arg
XM_006719614.2:c.8313C>G XP_006719677.1:p.Ser2771Arg
XM_006719616.2:c.8301C>G XP_006719679.1:p.Ser2767Arg
XM_011538770.1:c.8313C>G XP_011537072.1:p.Ser2771Arg
XM_011538771.1:c.8310C>G XP_011537073.1:p.Ser2770Arg
XM_011538772.1:c.8304C>G XP_011537074.1:p.Ser2768Arg
XM_011538773.1:c.8301C>G XP_011537075.1:p.Ser2767Arg
XM_011538774.1:c.8292C>G XP_011537076.1:p.Ser2764Arg
XM_011538775.1:c.8313C>G XP_011537077.1:p.Ser2771Arg
XM_011538776.1:c.8220C>G XP_011537078.1:p.Ser2740Arg
XR_944740.1:n.10633C>G
XM_005269162.4:c.8304C>G XP_005269219.1:p.Ser2768Arg
XM_006719614.4:c.8313C>G XP_006719677.1:p.Ser2771Arg
XM_006719616.3:c.8301C>G XP_006719679.1:p.Ser2767Arg
XM_011538770.2:c.8313C>G XP_011537072.1:p.Ser2771Arg
XM_011538771.2:c.8310C>G XP_011537073.1:p.Ser2770Arg
XM_011538772.2:c.8304C>G XP_011537074.1:p.Ser2768Arg
XM_011538773.2:c.8301C>G XP_011537075.1:p.Ser2767Arg
XM_011538774.2:c.8292C>G XP_011537076.1:p.Ser2764Arg
XM_011538776.2:c.8220C>G XP_011537078.1:p.Ser2740Arg
XR_001748874.1:n.9622C>G
NM_003482.4:c.8304C>G MANE Select NP_003473.3:p.Ser2768Arg