Canonical Allele Identifier: CA2034945531

Gene: KMT2D

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49030982C= , CM000674.2:g.49030982C=	GRCh38
NC_000012.11:g.49424765C= , CM000674.1:g.49424765C=	GRCh37
NC_000012.10:g.47711032C=	NCBI36
NG_027827.1:g.29343G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000552391.2:n.282G=
ENST00000683543.2:c.13582G=	ENSP00000506726.1:p.Ala4528=
ENST00000685166.1:c.13591G=	ENSP00000509386.1:p.Ala4531=
ENST00000685982.1:c.138+193G=	ENSP00000508613.1:n.138+193G=
ENST00000691986.1:c.138+193G=	ENSP00000509196.1:n.138+193G=
ENST00000692637.1:c.13579G=	ENSP00000509666.1:p.Ala4527=
ENST00000692973.1:c.183G=	ENSP00000508893.1:n.183G=
ENST00000301067.12:c.13582G= MANE Select	ENSP00000301067.7:p.Ala4528=
ENST00000301067.11:c.13582G=	ENSP00000301067.7:p.Ala4528=
ENST00000552391.1:n.282G=
NM_003482.3:c.13582G=	NP_003473.3:p.Ala4528=
XM_005269162.3:c.13582G=	XP_005269219.1:p.Ala4528=
XM_006719614.2:c.13591G=	XP_006719677.1:p.Ala4531=
XM_006719616.2:c.13579G=	XP_006719679.1:p.Ala4527=
XM_011538770.1:c.13591G=	XP_011537072.1:p.Ala4531=
XM_011538771.1:c.13588G=	XP_011537073.1:p.Ala4530=
XM_011538772.1:c.13582G=	XP_011537074.1:p.Ala4528=
XM_011538773.1:c.13579G=	XP_011537075.1:p.Ala4527=
XM_011538774.1:c.13570G=	XP_011537076.1:p.Ala4524=
XM_011538775.1:c.13591G=	XP_011537077.1:p.Ala4531=
XM_011538776.1:c.13498G=	XP_011537078.1:p.Ala4500=
XR_944740.1:n.15911G=
XM_005269162.4:c.13582G=	XP_005269219.1:p.Ala4528=
XM_006719614.4:c.13591G=	XP_006719677.1:p.Ala4531=
XM_006719616.3:c.13579G=	XP_006719679.1:p.Ala4527=
XM_011538770.2:c.13591G=	XP_011537072.1:p.Ala4531=
XM_011538771.2:c.13588G=	XP_011537073.1:p.Ala4530=
XM_011538772.2:c.13582G=	XP_011537074.1:p.Ala4528=
XM_011538773.2:c.13579G=	XP_011537075.1:p.Ala4527=
XM_011538774.2:c.13570G=	XP_011537076.1:p.Ala4524=
XM_011538776.2:c.13498G=	XP_011537078.1:p.Ala4500=
XR_001748874.1:n.14900G=
NM_003482.4:c.13582G= MANE Select	NP_003473.3:p.Ala4528=