Canonical Allele Identifier: CA384716721
Gene: KMT2D HGNC NCBI

Linked Data

ClinVar Variation Id: 3065270
ClinVar RCV Id: RCV003990347

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49033031G>A , CM000674.2:g.49033031G>A GRCh38
NC_000012.11:g.49426814G>A , CM000674.1:g.49426814G>A GRCh37
NC_000012.10:g.47713081G>A NCBI36
NG_027827.1:g.27294C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000683543.2:c.11674C>T ENSP00000506726.1:p.Gln3892Ter
ENST00000685166.1:c.11683C>T ENSP00000509386.1:p.Gln3895Ter
ENST00000685554.1:c.1234C>T ENSP00000508640.1:p.Gln412Ter
ENST00000687201.1:c.3253C>T ENSP00000510037.1:p.Gln1085Ter
ENST00000692637.1:c.11671C>T ENSP00000509666.1:p.Gln3891Ter
ENST00000692841.1:c.3153C>T ENSP00000508711.1:n.3153C>T
ENST00000301067.12:c.11674C>T MANE Select ENSP00000301067.7:p.Gln3892Ter
ENST00000301067.11:c.11674C>T ENSP00000301067.7:p.Gln3892Ter
NM_003482.3:c.11674C>T NP_003473.3:p.Gln3892Ter
XM_005269162.3:c.11674C>T XP_005269219.1:p.Gln3892Ter
XM_006719614.2:c.11683C>T XP_006719677.1:p.Gln3895Ter
XM_006719616.2:c.11671C>T XP_006719679.1:p.Gln3891Ter
XM_011538770.1:c.11683C>T XP_011537072.1:p.Gln3895Ter
XM_011538771.1:c.11680C>T XP_011537073.1:p.Gln3894Ter
XM_011538772.1:c.11674C>T XP_011537074.1:p.Gln3892Ter
XM_011538773.1:c.11671C>T XP_011537075.1:p.Gln3891Ter
XM_011538774.1:c.11662C>T XP_011537076.1:p.Gln3888Ter
XM_011538775.1:c.11683C>T XP_011537077.1:p.Gln3895Ter
XM_011538776.1:c.11590C>T XP_011537078.1:p.Gln3864Ter
XR_944740.1:n.14003C>T
XM_005269162.4:c.11674C>T XP_005269219.1:p.Gln3892Ter
XM_006719614.4:c.11683C>T XP_006719677.1:p.Gln3895Ter
XM_006719616.3:c.11671C>T XP_006719679.1:p.Gln3891Ter
XM_011538770.2:c.11683C>T XP_011537072.1:p.Gln3895Ter
XM_011538771.2:c.11680C>T XP_011537073.1:p.Gln3894Ter
XM_011538772.2:c.11674C>T XP_011537074.1:p.Gln3892Ter
XM_011538773.2:c.11671C>T XP_011537075.1:p.Gln3891Ter
XM_011538774.2:c.11662C>T XP_011537076.1:p.Gln3888Ter
XM_011538776.2:c.11590C>T XP_011537078.1:p.Gln3864Ter
XR_001748874.1:n.12992C>T
NM_003482.4:c.11674C>T MANE Select NP_003473.3:p.Gln3892Ter