Canonical Allele Identifier: CA2034958200
Gene: KMT2D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49048007C= , CM000674.2:g.49048007C= GRCh38
NC_000012.11:g.49441790C= , CM000674.1:g.49441790C= GRCh37
NC_000012.10:g.47728057C= NCBI36
NG_027827.1:g.12318G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000683543.2:c.4194G= ENSP00000506726.1:p.Ser1398=
ENST00000685166.1:c.4194G= ENSP00000509386.1:p.Ser1398=
ENST00000688095.1:c.174G= ENSP00000510007.1:p.Ser58=
ENST00000692637.1:c.4191G= ENSP00000509666.1:p.Ser1397=
ENST00000301067.12:c.4194G= MANE Select ENSP00000301067.7:p.Ser1398=
ENST00000301067.11:c.4194G= ENSP00000301067.7:p.Ser1398=
NM_003482.3:c.4194G= NP_003473.3:p.Ser1398=
XM_005269162.3:c.4194G= XP_005269219.1:p.Ser1398=
XM_006719614.2:c.4194G= XP_006719677.1:p.Ser1398=
XM_006719616.2:c.4191G= XP_006719679.1:p.Ser1397=
XM_011538770.1:c.4194G= XP_011537072.1:p.Ser1398=
XM_011538771.1:c.4191G= XP_011537073.1:p.Ser1397=
XM_011538772.1:c.4194G= XP_011537074.1:p.Ser1398=
XM_011538773.1:c.4191G= XP_011537075.1:p.Ser1397=
XM_011538774.1:c.4194G= XP_011537076.1:p.Ser1398=
XM_011538775.1:c.4194G= XP_011537077.1:p.Ser1398=
XM_011538776.1:c.4194G= XP_011537078.1:p.Ser1398=
XR_944740.1:n.6514G=
XM_005269162.4:c.4194G= XP_005269219.1:p.Ser1398=
XM_006719614.4:c.4194G= XP_006719677.1:p.Ser1398=
XM_006719616.3:c.4191G= XP_006719679.1:p.Ser1397=
XM_011538770.2:c.4194G= XP_011537072.1:p.Ser1398=
XM_011538771.2:c.4191G= XP_011537073.1:p.Ser1397=
XM_011538772.2:c.4194G= XP_011537074.1:p.Ser1398=
XM_011538773.2:c.4191G= XP_011537075.1:p.Ser1397=
XM_011538774.2:c.4194G= XP_011537076.1:p.Ser1398=
XM_011538776.2:c.4194G= XP_011537078.1:p.Ser1398=
XR_001748874.1:n.5503G=
NM_003482.4:c.4194G= MANE Select NP_003473.3:p.Ser1398=