Canonical Allele Identifier: CA2034963290
Gene: KMT2D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49022599G= , CM000674.2:g.49022599G= GRCh38
NC_000012.11:g.49416382G= , CM000674.1:g.49416382G= GRCh37
NC_000012.10:g.47702649G= NCBI36
NG_027827.1:g.37726C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000526209.2:c.299C=
ENST00000681974.1:n.1001C=
ENST00000682693.1:n.1963C=
ENST00000682886.1:n.499C=
ENST00000683543.2:c.16377C= ENSP00000506726.1:p.Tyr5459=
ENST00000683988.1:c.300C= ENSP00000506939.1:p.Tyr100=
ENST00000684428.1:c.864C= ENSP00000507433.1:p.Tyr288=
ENST00000684755.1:n.912C=
ENST00000685024.1:c.1483C=
ENST00000685166.1:c.16338C= ENSP00000509386.1:p.Tyr5446=
ENST00000688411.1:c.806C= ENSP00000510146.1:n.806C=
ENST00000691932.1:c.330C= ENSP00000509037.1:p.Tyr110=
ENST00000692637.1:c.16326C= ENSP00000509666.1:p.Tyr5442=
ENST00000301067.12:c.16329C= MANE Select ENSP00000301067.7:p.Tyr5443=
ENST00000301067.11:c.16329C= ENSP00000301067.7:p.Tyr5443=
ENST00000526209.1:c.372C= ENSP00000435714.1:p.Tyr124=
NM_003482.3:c.16329C= NP_003473.3:p.Tyr5443=
XM_005269162.3:c.16329C= XP_005269219.1:p.Tyr5443=
XM_006719614.2:c.16338C= XP_006719677.1:p.Tyr5446=
XM_006719616.2:c.16326C= XP_006719679.1:p.Tyr5442=
XM_011538770.1:c.16386C= XP_011537072.1:p.Tyr5462=
XM_011538771.1:c.16383C= XP_011537073.1:p.Tyr5461=
XM_011538772.1:c.16377C= XP_011537074.1:p.Tyr5459=
XM_011538773.1:c.16374C= XP_011537075.1:p.Tyr5458=
XM_011538774.1:c.16365C= XP_011537076.1:p.Tyr5455=
XM_011538775.1:c.16320C= XP_011537077.1:p.Tyr5440=
XM_011538776.1:c.16293C= XP_011537078.1:p.Tyr5431=
XM_005269162.4:c.16329C= XP_005269219.1:p.Tyr5443=
XM_006719614.4:c.16338C= XP_006719677.1:p.Tyr5446=
XM_006719616.3:c.16326C= XP_006719679.1:p.Tyr5442=
XM_011538770.2:c.16386C= XP_011537072.1:p.Tyr5462=
XM_011538771.2:c.16383C= XP_011537073.1:p.Tyr5461=
XM_011538772.2:c.16377C= XP_011537074.1:p.Tyr5459=
XM_011538773.2:c.16374C= XP_011537075.1:p.Tyr5458=
XM_011538774.2:c.16365C= XP_011537076.1:p.Tyr5455=
XM_011538776.2:c.16293C= XP_011537078.1:p.Tyr5431=
XR_001748874.1:n.16506C=
NM_003482.4:c.16329C= MANE Select NP_003473.3:p.Tyr5443=