Canonical Allele Identifier: CA2034959194
Gene: KMT2D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49039317A= , CM000674.2:g.49039317A= GRCh38
NC_000012.11:g.49433100A= , CM000674.1:g.49433100A= GRCh37
NC_000012.10:g.47719367A= NCBI36
NG_027827.1:g.21008T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000683543.2:c.8271T= ENSP00000506726.1:p.Ser2757=
ENST00000685166.1:c.8280T= ENSP00000509386.1:p.Ser2760=
ENST00000689060.1:c.2290T=
ENST00000689143.1:c.1944T= ENSP00000509839.1:p.Ser648=
ENST00000689944.1:c.2380T=
ENST00000692637.1:c.8268T= ENSP00000509666.1:p.Ser2756=
ENST00000301067.12:c.8271T= MANE Select ENSP00000301067.7:p.Ser2757=
ENST00000301067.11:c.8271T= ENSP00000301067.7:p.Ser2757=
NM_003482.3:c.8271T= NP_003473.3:p.Ser2757=
XM_005269162.3:c.8271T= XP_005269219.1:p.Ser2757=
XM_006719614.2:c.8280T= XP_006719677.1:p.Ser2760=
XM_006719616.2:c.8268T= XP_006719679.1:p.Ser2756=
XM_011538770.1:c.8280T= XP_011537072.1:p.Ser2760=
XM_011538771.1:c.8277T= XP_011537073.1:p.Ser2759=
XM_011538772.1:c.8271T= XP_011537074.1:p.Ser2757=
XM_011538773.1:c.8268T= XP_011537075.1:p.Ser2756=
XM_011538774.1:c.8259T= XP_011537076.1:p.Ser2753=
XM_011538775.1:c.8280T= XP_011537077.1:p.Ser2760=
XM_011538776.1:c.8187T= XP_011537078.1:p.Ser2729=
XR_944740.1:n.10600T=
XM_005269162.4:c.8271T= XP_005269219.1:p.Ser2757=
XM_006719614.4:c.8280T= XP_006719677.1:p.Ser2760=
XM_006719616.3:c.8268T= XP_006719679.1:p.Ser2756=
XM_011538770.2:c.8280T= XP_011537072.1:p.Ser2760=
XM_011538771.2:c.8277T= XP_011537073.1:p.Ser2759=
XM_011538772.2:c.8271T= XP_011537074.1:p.Ser2757=
XM_011538773.2:c.8268T= XP_011537075.1:p.Ser2756=
XM_011538774.2:c.8259T= XP_011537076.1:p.Ser2753=
XM_011538776.2:c.8187T= XP_011537078.1:p.Ser2729=
XR_001748874.1:n.9589T=
NM_003482.4:c.8271T= MANE Select NP_003473.3:p.Ser2757=