Canonical Allele Identifier: CA384708730
Gene: KMT2D HGNC NCBI

Linked Data

dbSNP Id: rs1045433904

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49031813T>A , CM000674.2:g.49031813T>A GRCh38
NC_000012.11:g.49425596T>A , CM000674.1:g.49425596T>A GRCh37
NC_000012.10:g.47711863T>A NCBI36
NG_027827.1:g.28512A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000683543.2:c.12892A>T ENSP00000506726.1:p.Thr4298Ser
ENST00000685166.1:c.12901A>T ENSP00000509386.1:p.Thr4301Ser
ENST00000685554.1:c.1753-501A>T ENSP00000508640.1:n.1753-501A>T
ENST00000692637.1:c.12889A>T ENSP00000509666.1:p.Thr4297Ser
ENST00000692841.1:c.4371A>T ENSP00000508711.1:n.4371A>T
ENST00000301067.12:c.12892A>T MANE Select ENSP00000301067.7:p.Thr4298Ser
ENST00000301067.11:c.12892A>T ENSP00000301067.7:p.Thr4298Ser
NM_003482.3:c.12892A>T NP_003473.3:p.Thr4298Ser
XM_005269162.3:c.12892A>T XP_005269219.1:p.Thr4298Ser
XM_006719614.2:c.12901A>T XP_006719677.1:p.Thr4301Ser
XM_006719616.2:c.12889A>T XP_006719679.1:p.Thr4297Ser
XM_011538770.1:c.12901A>T XP_011537072.1:p.Thr4301Ser
XM_011538771.1:c.12898A>T XP_011537073.1:p.Thr4300Ser
XM_011538772.1:c.12892A>T XP_011537074.1:p.Thr4298Ser
XM_011538773.1:c.12889A>T XP_011537075.1:p.Thr4297Ser
XM_011538774.1:c.12880A>T XP_011537076.1:p.Thr4294Ser
XM_011538775.1:c.12901A>T XP_011537077.1:p.Thr4301Ser
XM_011538776.1:c.12808A>T XP_011537078.1:p.Thr4270Ser
XR_944740.1:n.15221A>T
XM_005269162.4:c.12892A>T XP_005269219.1:p.Thr4298Ser
XM_006719614.4:c.12901A>T XP_006719677.1:p.Thr4301Ser
XM_006719616.3:c.12889A>T XP_006719679.1:p.Thr4297Ser
XM_011538770.2:c.12901A>T XP_011537072.1:p.Thr4301Ser
XM_011538771.2:c.12898A>T XP_011537073.1:p.Thr4300Ser
XM_011538772.2:c.12892A>T XP_011537074.1:p.Thr4298Ser
XM_011538773.2:c.12889A>T XP_011537075.1:p.Thr4297Ser
XM_011538774.2:c.12880A>T XP_011537076.1:p.Thr4294Ser
XM_011538776.2:c.12808A>T XP_011537078.1:p.Thr4270Ser
XR_001748874.1:n.14210A>T
NM_003482.4:c.12892A>T MANE Select NP_003473.3:p.Thr4298Ser