Canonical Allele Identifier: CA384628398
Gene: KMT2D HGNC NCBI

Linked Data

ClinVar Variation Id: 2757859
ClinVar RCV Id: RCV003590165
dbSNP Id: rs756972898

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49042627T>G , CM000674.2:g.49042627T>G GRCh38
NC_000012.11:g.49436410T>G , CM000674.1:g.49436410T>G GRCh37
NC_000012.10:g.47722677T>G NCBI36
NG_027827.1:g.17698A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650290.2:c.613A>C
ENST00000683543.2:c.5801A>C ENSP00000506726.1:p.Asn1934Thr
ENST00000685166.1:c.5810A>C ENSP00000509386.1:p.Asn1937Thr
ENST00000688095.1:c.1750A>C ENSP00000510007.1:n.1750A>C
ENST00000692637.1:c.5798A>C ENSP00000509666.1:p.Asn1933Thr
ENST00000301067.12:c.5801A>C MANE Select ENSP00000301067.7:p.Asn1934Thr
ENST00000301067.11:c.5801A>C ENSP00000301067.7:p.Asn1934Thr
NM_003482.3:c.5801A>C NP_003473.3:p.Asn1934Thr
XM_005269162.3:c.5801A>C XP_005269219.1:p.Asn1934Thr
XM_006719614.2:c.5810A>C XP_006719677.1:p.Asn1937Thr
XM_006719616.2:c.5798A>C XP_006719679.1:p.Asn1933Thr
XM_011538770.1:c.5810A>C XP_011537072.1:p.Asn1937Thr
XM_011538771.1:c.5807A>C XP_011537073.1:p.Asn1936Thr
XM_011538772.1:c.5801A>C XP_011537074.1:p.Asn1934Thr
XM_011538773.1:c.5798A>C XP_011537075.1:p.Asn1933Thr
XM_011538774.1:c.5810A>C XP_011537076.1:p.Asn1937Thr
XM_011538775.1:c.5810A>C XP_011537077.1:p.Asn1937Thr
XM_011538776.1:c.5810A>C XP_011537078.1:p.Asn1937Thr
XR_944740.1:n.8130A>C
XM_005269162.4:c.5801A>C XP_005269219.1:p.Asn1934Thr
XM_006719614.4:c.5810A>C XP_006719677.1:p.Asn1937Thr
XM_006719616.3:c.5798A>C XP_006719679.1:p.Asn1933Thr
XM_011538770.2:c.5810A>C XP_011537072.1:p.Asn1937Thr
XM_011538771.2:c.5807A>C XP_011537073.1:p.Asn1936Thr
XM_011538772.2:c.5801A>C XP_011537074.1:p.Asn1934Thr
XM_011538773.2:c.5798A>C XP_011537075.1:p.Asn1933Thr
XM_011538774.2:c.5810A>C XP_011537076.1:p.Asn1937Thr
XM_011538776.2:c.5810A>C XP_011537078.1:p.Asn1937Thr
XR_001748874.1:n.7119A>C
NM_003482.4:c.5801A>C MANE Select NP_003473.3:p.Asn1934Thr