Canonical Allele Identifier: CA2034964177

Gene: KMT2D

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49024841G= , CM000674.2:g.49024841G=	GRCh38
NC_000012.11:g.49418624G= , CM000674.1:g.49418624G=	GRCh37
NC_000012.10:g.47704891G=	NCBI36
NG_027827.1:g.35484C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681974.1:n.562C=
ENST00000683543.2:c.15890C=	ENSP00000506726.1:p.Thr5297=
ENST00000683863.1:n.1605C=
ENST00000684428.1:c.425C=	ENSP00000507433.1:p.Thr142=
ENST00000684755.1:n.425C=
ENST00000685024.1:c.1015C=
ENST00000685166.1:c.15899C=	ENSP00000509386.1:p.Thr5300=
ENST00000688411.1:c.367C=	ENSP00000510146.1:n.367C=
ENST00000691463.1:c.1276C=	ENSP00000510624.1:n.1276C=
ENST00000692637.1:c.15887C=	ENSP00000509666.1:p.Thr5296=
ENST00000301067.12:c.15890C= MANE Select	ENSP00000301067.7:p.Thr5297=
ENST00000301067.11:c.15890C=	ENSP00000301067.7:p.Thr5297=
NM_003482.3:c.15890C=	NP_003473.3:p.Thr5297=
XM_005269162.3:c.15890C=	XP_005269219.1:p.Thr5297=
XM_006719614.2:c.15899C=	XP_006719677.1:p.Thr5300=
XM_006719616.2:c.15887C=	XP_006719679.1:p.Thr5296=
XM_011538770.1:c.15899C=	XP_011537072.1:p.Thr5300=
XM_011538771.1:c.15896C=	XP_011537073.1:p.Thr5299=
XM_011538772.1:c.15890C=	XP_011537074.1:p.Thr5297=
XM_011538773.1:c.15887C=	XP_011537075.1:p.Thr5296=
XM_011538774.1:c.15878C=	XP_011537076.1:p.Thr5293=
XM_011538775.1:c.15833C=	XP_011537077.1:p.Thr5278=
XM_011538776.1:c.15806C=	XP_011537078.1:p.Thr5269=
XR_944740.1:n.17078C=
XM_005269162.4:c.15890C=	XP_005269219.1:p.Thr5297=
XM_006719614.4:c.15899C=	XP_006719677.1:p.Thr5300=
XM_006719616.3:c.15887C=	XP_006719679.1:p.Thr5296=
XM_011538770.2:c.15899C=	XP_011537072.1:p.Thr5300=
XM_011538771.2:c.15896C=	XP_011537073.1:p.Thr5299=
XM_011538772.2:c.15890C=	XP_011537074.1:p.Thr5297=
XM_011538773.2:c.15887C=	XP_011537075.1:p.Thr5296=
XM_011538774.2:c.15878C=	XP_011537076.1:p.Thr5293=
XM_011538776.2:c.15806C=	XP_011537078.1:p.Thr5269=
XR_001748874.1:n.16067C=
NM_003482.4:c.15890C= MANE Select	NP_003473.3:p.Thr5297=