Canonical Allele Identifier: CA479521962
Gene: KMT2D HGNC NCBI

Linked Data

dbSNP Id: rs1357775506
MyVariant Identifiers: chr12:g.49418605G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49024822G>A , CM000674.2:g.49024822G>A GRCh38
NC_000012.11:g.49418605G>A , CM000674.1:g.49418605G>A GRCh37
NC_000012.10:g.47704872G>A NCBI36
NG_027827.1:g.35503C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000681974.1:n.581C>T
ENST00000683543.2:c.15909C>T ENSP00000506726.1:p.Arg5303=
ENST00000683863.1:n.1624C>T
ENST00000684428.1:c.444C>T ENSP00000507433.1:p.Arg148=
ENST00000684755.1:n.444C>T
ENST00000685024.1:c.1034C>T
ENST00000685166.1:c.15918C>T ENSP00000509386.1:p.Arg5306=
ENST00000688411.1:c.386C>T ENSP00000510146.1:n.386C>T
ENST00000691463.1:c.1295C>T ENSP00000510624.1:n.1295C>T
ENST00000692637.1:c.15906C>T ENSP00000509666.1:p.Arg5302=
ENST00000301067.12:c.15909C>T MANE Select ENSP00000301067.7:p.Arg5303=
ENST00000301067.11:c.15909C>T ENSP00000301067.7:p.Arg5303=
NM_003482.3:c.15909C>T NP_003473.3:p.Arg5303=
XM_005269162.3:c.15909C>T XP_005269219.1:p.Arg5303=
XM_006719614.2:c.15918C>T XP_006719677.1:p.Arg5306=
XM_006719616.2:c.15906C>T XP_006719679.1:p.Arg5302=
XM_011538770.1:c.15918C>T XP_011537072.1:p.Arg5306=
XM_011538771.1:c.15915C>T XP_011537073.1:p.Arg5305=
XM_011538772.1:c.15909C>T XP_011537074.1:p.Arg5303=
XM_011538773.1:c.15906C>T XP_011537075.1:p.Arg5302=
XM_011538774.1:c.15897C>T XP_011537076.1:p.Arg5299=
XM_011538775.1:c.15852C>T XP_011537077.1:p.Arg5284=
XM_011538776.1:c.15825C>T XP_011537078.1:p.Arg5275=
XR_944740.1:n.17097C>T
XM_005269162.4:c.15909C>T XP_005269219.1:p.Arg5303=
XM_006719614.4:c.15918C>T XP_006719677.1:p.Arg5306=
XM_006719616.3:c.15906C>T XP_006719679.1:p.Arg5302=
XM_011538770.2:c.15918C>T XP_011537072.1:p.Arg5306=
XM_011538771.2:c.15915C>T XP_011537073.1:p.Arg5305=
XM_011538772.2:c.15909C>T XP_011537074.1:p.Arg5303=
XM_011538773.2:c.15906C>T XP_011537075.1:p.Arg5302=
XM_011538774.2:c.15897C>T XP_011537076.1:p.Arg5299=
XM_011538776.2:c.15825C>T XP_011537078.1:p.Arg5275=
XR_001748874.1:n.16086C>T
NM_003482.4:c.15909C>T MANE Select NP_003473.3:p.Arg5303=