Canonical Allele Identifier: CA2034945534

Gene: KMT2D

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49030986C= , CM000674.2:g.49030986C=	GRCh38
NC_000012.11:g.49424769C= , CM000674.1:g.49424769C=	GRCh37
NC_000012.10:g.47711036C=	NCBI36
NG_027827.1:g.29339G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000552391.2:n.278G=
ENST00000683543.2:c.13578G=	ENSP00000506726.1:p.Gln4526=
ENST00000685166.1:c.13587G=	ENSP00000509386.1:p.Gln4529=
ENST00000685982.1:c.138+189G=	ENSP00000508613.1:n.138+189G=
ENST00000691986.1:c.138+189G=	ENSP00000509196.1:n.138+189G=
ENST00000692637.1:c.13575G=	ENSP00000509666.1:p.Gln4525=
ENST00000692973.1:c.179G=	ENSP00000508893.1:n.179G=
ENST00000301067.12:c.13578G= MANE Select	ENSP00000301067.7:p.Gln4526=
ENST00000301067.11:c.13578G=	ENSP00000301067.7:p.Gln4526=
ENST00000552391.1:n.278G=
NM_003482.3:c.13578G=	NP_003473.3:p.Gln4526=
XM_005269162.3:c.13578G=	XP_005269219.1:p.Gln4526=
XM_006719614.2:c.13587G=	XP_006719677.1:p.Gln4529=
XM_006719616.2:c.13575G=	XP_006719679.1:p.Gln4525=
XM_011538770.1:c.13587G=	XP_011537072.1:p.Gln4529=
XM_011538771.1:c.13584G=	XP_011537073.1:p.Gln4528=
XM_011538772.1:c.13578G=	XP_011537074.1:p.Gln4526=
XM_011538773.1:c.13575G=	XP_011537075.1:p.Gln4525=
XM_011538774.1:c.13566G=	XP_011537076.1:p.Gln4522=
XM_011538775.1:c.13587G=	XP_011537077.1:p.Gln4529=
XM_011538776.1:c.13494G=	XP_011537078.1:p.Gln4498=
XR_944740.1:n.15907G=
XM_005269162.4:c.13578G=	XP_005269219.1:p.Gln4526=
XM_006719614.4:c.13587G=	XP_006719677.1:p.Gln4529=
XM_006719616.3:c.13575G=	XP_006719679.1:p.Gln4525=
XM_011538770.2:c.13587G=	XP_011537072.1:p.Gln4529=
XM_011538771.2:c.13584G=	XP_011537073.1:p.Gln4528=
XM_011538772.2:c.13578G=	XP_011537074.1:p.Gln4526=
XM_011538773.2:c.13575G=	XP_011537075.1:p.Gln4525=
XM_011538774.2:c.13566G=	XP_011537076.1:p.Gln4522=
XM_011538776.2:c.13494G=	XP_011537078.1:p.Gln4498=
XR_001748874.1:n.14896G=
NM_003482.4:c.13578G= MANE Select	NP_003473.3:p.Gln4526=