Canonical Allele Identifier: CA384743045
Gene: KMT2D HGNC NCBI

Linked Data

dbSNP Id: rs374075728

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49039328T>A , CM000674.2:g.49039328T>A GRCh38
NC_000012.11:g.49433111T>A , CM000674.1:g.49433111T>A GRCh37
NC_000012.10:g.47719378T>A NCBI36
NG_027827.1:g.20997A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000683543.2:c.8260A>T ENSP00000506726.1:p.Ser2754Cys
ENST00000685166.1:c.8269A>T ENSP00000509386.1:p.Ser2757Cys
ENST00000689060.1:c.2279A>T
ENST00000689143.1:c.1933A>T ENSP00000509839.1:p.Ser645Cys
ENST00000689944.1:c.2369A>T
ENST00000692637.1:c.8257A>T ENSP00000509666.1:p.Ser2753Cys
ENST00000301067.12:c.8260A>T MANE Select ENSP00000301067.7:p.Ser2754Cys
ENST00000301067.11:c.8260A>T ENSP00000301067.7:p.Ser2754Cys
NM_003482.3:c.8260A>T NP_003473.3:p.Ser2754Cys
XM_005269162.3:c.8260A>T XP_005269219.1:p.Ser2754Cys
XM_006719614.2:c.8269A>T XP_006719677.1:p.Ser2757Cys
XM_006719616.2:c.8257A>T XP_006719679.1:p.Ser2753Cys
XM_011538770.1:c.8269A>T XP_011537072.1:p.Ser2757Cys
XM_011538771.1:c.8266A>T XP_011537073.1:p.Ser2756Cys
XM_011538772.1:c.8260A>T XP_011537074.1:p.Ser2754Cys
XM_011538773.1:c.8257A>T XP_011537075.1:p.Ser2753Cys
XM_011538774.1:c.8248A>T XP_011537076.1:p.Ser2750Cys
XM_011538775.1:c.8269A>T XP_011537077.1:p.Ser2757Cys
XM_011538776.1:c.8176A>T XP_011537078.1:p.Ser2726Cys
XR_944740.1:n.10589A>T
XM_005269162.4:c.8260A>T XP_005269219.1:p.Ser2754Cys
XM_006719614.4:c.8269A>T XP_006719677.1:p.Ser2757Cys
XM_006719616.3:c.8257A>T XP_006719679.1:p.Ser2753Cys
XM_011538770.2:c.8269A>T XP_011537072.1:p.Ser2757Cys
XM_011538771.2:c.8266A>T XP_011537073.1:p.Ser2756Cys
XM_011538772.2:c.8260A>T XP_011537074.1:p.Ser2754Cys
XM_011538773.2:c.8257A>T XP_011537075.1:p.Ser2753Cys
XM_011538774.2:c.8248A>T XP_011537076.1:p.Ser2750Cys
XM_011538776.2:c.8176A>T XP_011537078.1:p.Ser2726Cys
XR_001748874.1:n.9578A>T
NM_003482.4:c.8260A>T MANE Select NP_003473.3:p.Ser2754Cys