Canonical Allele Identifier: CA2034945507

Gene: KMT2D

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49030934C= , CM000674.2:g.49030934C=	GRCh38
NC_000012.11:g.49424717C= , CM000674.1:g.49424717C=	GRCh37
NC_000012.10:g.47710984C=	NCBI36
NG_027827.1:g.29391G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000552391.2:n.330G=
ENST00000683543.2:c.13630G=	ENSP00000506726.1:p.Gly4544=
ENST00000685166.1:c.13639G=	ENSP00000509386.1:p.Gly4547=
ENST00000685982.1:c.139-166G=	ENSP00000508613.1:n.139-166G=
ENST00000691986.1:c.138+241G=	ENSP00000509196.1:n.138+241G=
ENST00000692637.1:c.13627G=	ENSP00000509666.1:p.Gly4543=
ENST00000692973.1:c.231G=	ENSP00000508893.1:n.231G=
ENST00000301067.12:c.13630G= MANE Select	ENSP00000301067.7:p.Gly4544=
ENST00000301067.11:c.13630G=	ENSP00000301067.7:p.Gly4544=
ENST00000552391.1:n.330G=
NM_003482.3:c.13630G=	NP_003473.3:p.Gly4544=
XM_005269162.3:c.13630G=	XP_005269219.1:p.Gly4544=
XM_006719614.2:c.13639G=	XP_006719677.1:p.Gly4547=
XM_006719616.2:c.13627G=	XP_006719679.1:p.Gly4543=
XM_011538770.1:c.13639G=	XP_011537072.1:p.Gly4547=
XM_011538771.1:c.13636G=	XP_011537073.1:p.Gly4546=
XM_011538772.1:c.13630G=	XP_011537074.1:p.Gly4544=
XM_011538773.1:c.13627G=	XP_011537075.1:p.Gly4543=
XM_011538774.1:c.13618G=	XP_011537076.1:p.Gly4540=
XM_011538775.1:c.13639G=	XP_011537077.1:p.Gly4547=
XM_011538776.1:c.13546G=	XP_011537078.1:p.Gly4516=
XR_944740.1:n.15959G=
XM_005269162.4:c.13630G=	XP_005269219.1:p.Gly4544=
XM_006719614.4:c.13639G=	XP_006719677.1:p.Gly4547=
XM_006719616.3:c.13627G=	XP_006719679.1:p.Gly4543=
XM_011538770.2:c.13639G=	XP_011537072.1:p.Gly4547=
XM_011538771.2:c.13636G=	XP_011537073.1:p.Gly4546=
XM_011538772.2:c.13630G=	XP_011537074.1:p.Gly4544=
XM_011538773.2:c.13627G=	XP_011537075.1:p.Gly4543=
XM_011538774.2:c.13618G=	XP_011537076.1:p.Gly4540=
XM_011538776.2:c.13546G=	XP_011537078.1:p.Gly4516=
XR_001748874.1:n.14948G=
NM_003482.4:c.13630G= MANE Select	NP_003473.3:p.Gly4544=