Canonical Allele Identifier: CA275235
Gene: KMT2D HGNC NCBI

Linked Data

ClinVar Variation Id: 197074
ClinVar RCV Id: RCV000177995
dbSNP Id: rs794727610

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49032766del , CM000674.2:g.49032766del GRCh38
NC_000012.11:g.49426549del , CM000674.1:g.49426549del GRCh37
NC_000012.10:g.47712816del NCBI36
NG_027827.1:g.27559del

Transcript Alleles

HGVS Amino-acid Change
ENST00000683543.2:c.11939del ENSP00000506726.1:p.Gln3980ArgfsTer?
ENST00000685166.1:c.11948del ENSP00000509386.1:p.Gln3983ArgfsTer?
ENST00000685554.1:c.1499del ENSP00000508640.1:p.Gln500ArgfsTer?
ENST00000687201.1:c.3518del ENSP00000510037.1:p.Gln1173ArgfsTer?
ENST00000692637.1:c.11936del ENSP00000509666.1:p.Gln3979ArgfsTer?
ENST00000692841.1:c.3418del ENSP00000508711.1:n.3418del
ENST00000301067.12:c.11939del MANE Select ENSP00000301067.7:p.Gln3980ArgfsTer?
ENST00000301067.11:c.11939del ENSP00000301067.7:p.Gln3980ArgfsTer?
NM_003482.3:c.11939del NP_003473.3:p.Gln3980ArgfsTer?
XM_005269162.3:c.11939del XP_005269219.1:p.Gln3980ArgfsTer?
XM_006719614.2:c.11948del XP_006719677.1:p.Gln3983ArgfsTer?
XM_006719616.2:c.11936del XP_006719679.1:p.Gln3979ArgfsTer?
XM_011538770.1:c.11948del XP_011537072.1:p.Gln3983ArgfsTer?
XM_011538771.1:c.11945del XP_011537073.1:p.Gln3982ArgfsTer?
XM_011538772.1:c.11939del XP_011537074.1:p.Gln3980ArgfsTer?
XM_011538773.1:c.11936del XP_011537075.1:p.Gln3979ArgfsTer?
XM_011538774.1:c.11927del XP_011537076.1:p.Gln3976ArgfsTer?
XM_011538775.1:c.11948del XP_011537077.1:p.Gln3983ArgfsTer?
XM_011538776.1:c.11855del XP_011537078.1:p.Gln3952ArgfsTer?
XR_944740.1:n.14268del
XM_005269162.4:c.11939del XP_005269219.1:p.Gln3980ArgfsTer?
XM_006719614.4:c.11948del XP_006719677.1:p.Gln3983ArgfsTer?
XM_006719616.3:c.11936del XP_006719679.1:p.Gln3979ArgfsTer?
XM_011538770.2:c.11948del XP_011537072.1:p.Gln3983ArgfsTer?
XM_011538771.2:c.11945del XP_011537073.1:p.Gln3982ArgfsTer?
XM_011538772.2:c.11939del XP_011537074.1:p.Gln3980ArgfsTer?
XM_011538773.2:c.11936del XP_011537075.1:p.Gln3979ArgfsTer?
XM_011538774.2:c.11927del XP_011537076.1:p.Gln3976ArgfsTer?
XM_011538776.2:c.11855del XP_011537078.1:p.Gln3952ArgfsTer?
XR_001748874.1:n.13257del
NM_003482.4:c.11939del MANE Select NP_003473.3:p.Gln3980ArgfsTer?