Canonical Allele Identifier: CA2034946021
Gene: KMT2D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49031922A= , CM000674.2:g.49031922A= GRCh38
NC_000012.11:g.49425705A= , CM000674.1:g.49425705A= GRCh37
NC_000012.10:g.47711972A= NCBI36
NG_027827.1:g.28403T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000683543.2:c.12783T= ENSP00000506726.1:p.Pro4261=
ENST00000685166.1:c.12792T= ENSP00000509386.1:p.Pro4264=
ENST00000685554.1:c.1752+591T= ENSP00000508640.1:n.1752+591T=
ENST00000692637.1:c.12780T= ENSP00000509666.1:p.Pro4260=
ENST00000692841.1:c.4262T= ENSP00000508711.1:n.4262T=
ENST00000301067.12:c.12783T= MANE Select ENSP00000301067.7:p.Pro4261=
ENST00000301067.11:c.12783T= ENSP00000301067.7:p.Pro4261=
NM_003482.3:c.12783T= NP_003473.3:p.Pro4261=
XM_005269162.3:c.12783T= XP_005269219.1:p.Pro4261=
XM_006719614.2:c.12792T= XP_006719677.1:p.Pro4264=
XM_006719616.2:c.12780T= XP_006719679.1:p.Pro4260=
XM_011538770.1:c.12792T= XP_011537072.1:p.Pro4264=
XM_011538771.1:c.12789T= XP_011537073.1:p.Pro4263=
XM_011538772.1:c.12783T= XP_011537074.1:p.Pro4261=
XM_011538773.1:c.12780T= XP_011537075.1:p.Pro4260=
XM_011538774.1:c.12771T= XP_011537076.1:p.Pro4257=
XM_011538775.1:c.12792T= XP_011537077.1:p.Pro4264=
XM_011538776.1:c.12699T= XP_011537078.1:p.Pro4233=
XR_944740.1:n.15112T=
XM_005269162.4:c.12783T= XP_005269219.1:p.Pro4261=
XM_006719614.4:c.12792T= XP_006719677.1:p.Pro4264=
XM_006719616.3:c.12780T= XP_006719679.1:p.Pro4260=
XM_011538770.2:c.12792T= XP_011537072.1:p.Pro4264=
XM_011538771.2:c.12789T= XP_011537073.1:p.Pro4263=
XM_011538772.2:c.12783T= XP_011537074.1:p.Pro4261=
XM_011538773.2:c.12780T= XP_011537075.1:p.Pro4260=
XM_011538774.2:c.12771T= XP_011537076.1:p.Pro4257=
XM_011538776.2:c.12699T= XP_011537078.1:p.Pro4233=
XR_001748874.1:n.14101T=
NM_003482.4:c.12783T= MANE Select NP_003473.3:p.Pro4261=