Canonical Allele Identifier: CA2034945533

Gene: KMT2D

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49030985T= , CM000674.2:g.49030985T=	GRCh38
NC_000012.11:g.49424768T= , CM000674.1:g.49424768T=	GRCh37
NC_000012.10:g.47711035T=	NCBI36
NG_027827.1:g.29340A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000552391.2:n.279A=
ENST00000683543.2:c.13579A=	ENSP00000506726.1:p.Lys4527=
ENST00000685166.1:c.13588A=	ENSP00000509386.1:p.Lys4530=
ENST00000685982.1:c.138+190A=	ENSP00000508613.1:n.138+190A=
ENST00000691986.1:c.138+190A=	ENSP00000509196.1:n.138+190A=
ENST00000692637.1:c.13576A=	ENSP00000509666.1:p.Lys4526=
ENST00000692973.1:c.180A=	ENSP00000508893.1:n.180A=
ENST00000301067.12:c.13579A= MANE Select	ENSP00000301067.7:p.Lys4527=
ENST00000301067.11:c.13579A=	ENSP00000301067.7:p.Lys4527=
ENST00000552391.1:n.279A=
NM_003482.3:c.13579A=	NP_003473.3:p.Lys4527=
XM_005269162.3:c.13579A=	XP_005269219.1:p.Lys4527=
XM_006719614.2:c.13588A=	XP_006719677.1:p.Lys4530=
XM_006719616.2:c.13576A=	XP_006719679.1:p.Lys4526=
XM_011538770.1:c.13588A=	XP_011537072.1:p.Lys4530=
XM_011538771.1:c.13585A=	XP_011537073.1:p.Lys4529=
XM_011538772.1:c.13579A=	XP_011537074.1:p.Lys4527=
XM_011538773.1:c.13576A=	XP_011537075.1:p.Lys4526=
XM_011538774.1:c.13567A=	XP_011537076.1:p.Lys4523=
XM_011538775.1:c.13588A=	XP_011537077.1:p.Lys4530=
XM_011538776.1:c.13495A=	XP_011537078.1:p.Lys4499=
XR_944740.1:n.15908A=
XM_005269162.4:c.13579A=	XP_005269219.1:p.Lys4527=
XM_006719614.4:c.13588A=	XP_006719677.1:p.Lys4530=
XM_006719616.3:c.13576A=	XP_006719679.1:p.Lys4526=
XM_011538770.2:c.13588A=	XP_011537072.1:p.Lys4530=
XM_011538771.2:c.13585A=	XP_011537073.1:p.Lys4529=
XM_011538772.2:c.13579A=	XP_011537074.1:p.Lys4527=
XM_011538773.2:c.13576A=	XP_011537075.1:p.Lys4526=
XM_011538774.2:c.13567A=	XP_011537076.1:p.Lys4523=
XM_011538776.2:c.13495A=	XP_011537078.1:p.Lys4499=
XR_001748874.1:n.14897A=
NM_003482.4:c.13579A= MANE Select	NP_003473.3:p.Lys4527=