Canonical Allele Identifier: CA2034948359

Gene: KMT2D

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49042604C= , CM000674.2:g.49042604C=	GRCh38
NC_000012.11:g.49436387C= , CM000674.1:g.49436387C=	GRCh37
NC_000012.10:g.47722654C=	NCBI36
NG_027827.1:g.17721G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650290.2:c.636G=
ENST00000683543.2:c.5824G=	ENSP00000506726.1:p.Asp1942=
ENST00000685166.1:c.5833G=	ENSP00000509386.1:p.Asp1945=
ENST00000688095.1:c.1773G=	ENSP00000510007.1:n.1773G=
ENST00000692637.1:c.5821G=	ENSP00000509666.1:p.Asp1941=
ENST00000301067.12:c.5824G= MANE Select	ENSP00000301067.7:p.Asp1942=
ENST00000301067.11:c.5824G=	ENSP00000301067.7:p.Asp1942=
NM_003482.3:c.5824G=	NP_003473.3:p.Asp1942=
XM_005269162.3:c.5824G=	XP_005269219.1:p.Asp1942=
XM_006719614.2:c.5833G=	XP_006719677.1:p.Asp1945=
XM_006719616.2:c.5821G=	XP_006719679.1:p.Asp1941=
XM_011538770.1:c.5833G=	XP_011537072.1:p.Asp1945=
XM_011538771.1:c.5830G=	XP_011537073.1:p.Asp1944=
XM_011538772.1:c.5824G=	XP_011537074.1:p.Asp1942=
XM_011538773.1:c.5821G=	XP_011537075.1:p.Asp1941=
XM_011538774.1:c.5833G=	XP_011537076.1:p.Asp1945=
XM_011538775.1:c.5833G=	XP_011537077.1:p.Asp1945=
XM_011538776.1:c.5833G=	XP_011537078.1:p.Asp1945=
XR_944740.1:n.8153G=
XM_005269162.4:c.5824G=	XP_005269219.1:p.Asp1942=
XM_006719614.4:c.5833G=	XP_006719677.1:p.Asp1945=
XM_006719616.3:c.5821G=	XP_006719679.1:p.Asp1941=
XM_011538770.2:c.5833G=	XP_011537072.1:p.Asp1945=
XM_011538771.2:c.5830G=	XP_011537073.1:p.Asp1944=
XM_011538772.2:c.5824G=	XP_011537074.1:p.Asp1942=
XM_011538773.2:c.5821G=	XP_011537075.1:p.Asp1941=
XM_011538774.2:c.5833G=	XP_011537076.1:p.Asp1945=
XM_011538776.2:c.5833G=	XP_011537078.1:p.Asp1945=
XR_001748874.1:n.7142G=
NM_003482.4:c.5824G= MANE Select	NP_003473.3:p.Asp1942=