Canonical Allele Identifier: CA645579666
Gene: KMT2D HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49039434_49039435delinsAA , CM000674.2:g.49039434_49039435delinsAA GRCh38
NC_000012.11:g.49433217_49433218delinsAA , CM000674.1:g.49433217_49433218delinsAA GRCh37
NC_000012.10:g.47719484_47719485delinsAA NCBI36
NG_027827.1:g.20890_20891delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000683543.2:c.8229_8229+1delinsTT
ENST00000685166.1:c.8238_8238+1delinsTT
ENST00000689060.1:c.2248_2248+1delinsTT
ENST00000689143.1:c.1902_1902+1delinsTT
ENST00000689944.1:c.2338_2338+1delinsTT
ENST00000692637.1:c.8226_8226+1delinsTT
ENST00000301067.12:c.8229_8229+1delinsTT
ENST00000301067.11:c.8229_8229+1delinsTT
NM_003482.3:c.8229_8229+1delinsTT
XM_005269162.3:c.8229_8229+1delinsTT
XM_006719614.2:c.8238_8238+1delinsTT
XM_006719616.2:c.8226_8226+1delinsTT
XM_011538770.1:c.8238_8238+1delinsTT
XM_011538771.1:c.8235_8235+1delinsTT
XM_011538772.1:c.8229_8229+1delinsTT
XM_011538773.1:c.8226_8226+1delinsTT
XM_011538774.1:c.8217_8217+1delinsTT
XM_011538775.1:c.8238_8238+1delinsTT
XM_011538776.1:c.8145_8145+1delinsTT
XR_944740.1:n.10558_10558+1delinsTT
XM_005269162.4:c.8229_8229+1delinsTT
XM_006719614.4:c.8238_8238+1delinsTT
XM_006719616.3:c.8226_8226+1delinsTT
XM_011538770.2:c.8238_8238+1delinsTT
XM_011538771.2:c.8235_8235+1delinsTT
XM_011538772.2:c.8229_8229+1delinsTT
XM_011538773.2:c.8226_8226+1delinsTT
XM_011538774.2:c.8217_8217+1delinsTT
XM_011538776.2:c.8145_8145+1delinsTT
XR_001748874.1:n.9547_9547+1delinsTT
NM_003482.4:c.8229_8229+1delinsTT