Canonical Allele Identifier: CA2034963286
Gene: KMT2D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49022591T= , CM000674.2:g.49022591T= GRCh38
NC_000012.11:g.49416374T= , CM000674.1:g.49416374T= GRCh37
NC_000012.10:g.47702641T= NCBI36
NG_027827.1:g.37734A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000526209.2:c.307A=
ENST00000681974.1:n.1009A=
ENST00000682693.1:n.1971A=
ENST00000682886.1:n.507A=
ENST00000683543.2:c.16385A= ENSP00000506726.1:p.Gln5462=
ENST00000683988.1:c.308A= ENSP00000506939.1:p.Gln103=
ENST00000684428.1:c.872A= ENSP00000507433.1:p.Gln291=
ENST00000684755.1:n.920A=
ENST00000685024.1:c.1491A=
ENST00000685166.1:c.16346A= ENSP00000509386.1:p.Gln5449=
ENST00000688411.1:c.814A= ENSP00000510146.1:n.814A=
ENST00000691932.1:c.338A= ENSP00000509037.1:p.Gln113=
ENST00000692637.1:c.16334A= ENSP00000509666.1:p.Gln5445=
ENST00000301067.12:c.16337A= MANE Select ENSP00000301067.7:p.Gln5446=
ENST00000301067.11:c.16337A= ENSP00000301067.7:p.Gln5446=
ENST00000526209.1:c.380A= ENSP00000435714.1:p.Gln127=
NM_003482.3:c.16337A= NP_003473.3:p.Gln5446=
XM_005269162.3:c.16337A= XP_005269219.1:p.Gln5446=
XM_006719614.2:c.16346A= XP_006719677.1:p.Gln5449=
XM_006719616.2:c.16334A= XP_006719679.1:p.Gln5445=
XM_011538770.1:c.16394A= XP_011537072.1:p.Gln5465=
XM_011538771.1:c.16391A= XP_011537073.1:p.Gln5464=
XM_011538772.1:c.16385A= XP_011537074.1:p.Gln5462=
XM_011538773.1:c.16382A= XP_011537075.1:p.Gln5461=
XM_011538774.1:c.16373A= XP_011537076.1:p.Gln5458=
XM_011538775.1:c.16328A= XP_011537077.1:p.Gln5443=
XM_011538776.1:c.16301A= XP_011537078.1:p.Gln5434=
XM_005269162.4:c.16337A= XP_005269219.1:p.Gln5446=
XM_006719614.4:c.16346A= XP_006719677.1:p.Gln5449=
XM_006719616.3:c.16334A= XP_006719679.1:p.Gln5445=
XM_011538770.2:c.16394A= XP_011537072.1:p.Gln5465=
XM_011538771.2:c.16391A= XP_011537073.1:p.Gln5464=
XM_011538772.2:c.16385A= XP_011537074.1:p.Gln5462=
XM_011538773.2:c.16382A= XP_011537075.1:p.Gln5461=
XM_011538774.2:c.16373A= XP_011537076.1:p.Gln5458=
XM_011538776.2:c.16301A= XP_011537078.1:p.Gln5434=
XR_001748874.1:n.16514A=
NM_003482.4:c.16337A= MANE Select NP_003473.3:p.Gln5446=