Canonical Allele Identifier: CA2034963248

Gene: KMT2D

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49022500T= , CM000674.2:g.49022500T=	GRCh38
NC_000012.11:g.49416283T= , CM000674.1:g.49416283T=	GRCh37
NC_000012.10:g.47702550T=	NCBI36
NG_027827.1:g.37825A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526209.2:c.308+90A=
ENST00000681974.1:n.1010+90A=
ENST00000682693.1:n.1972+90A=
ENST00000682886.1:n.598A=
ENST00000683543.2:c.16386+90A=	ENSP00000506726.1:n.16386+90A=
ENST00000683988.1:c.309+90A=	ENSP00000506939.1:n.309+90A=
ENST00000684428.1:c.874-89A=	ENSP00000507433.1:n.874-89A=
ENST00000685024.1:c.1492+90A=
ENST00000685166.1:c.16347+90A=	ENSP00000509386.1:n.16347+90A=
ENST00000691932.1:c.339+90A=	ENSP00000509037.1:n.339+90A=
ENST00000692637.1:c.16335+90A=	ENSP00000509666.1:n.16335+90A=
ENST00000301067.12:c.16338+90A= MANE Select	ENSP00000301067.7:n.16338+90A=
ENST00000301067.11:c.16338+90A=	ENSP00000301067.7:n.16338+90A=
ENST00000526209.1:c.381+90A=	ENSP00000435714.1:n.381+90A=
NM_003482.3:c.16338+90A=	NP_003473.3:n.16338+90A=
XM_005269162.3:c.16338+90A=	XP_005269219.1:n.16338+90A=
XM_006719614.2:c.16347+90A=	XP_006719677.1:n.16347+90A=
XM_006719616.2:c.16335+90A=	XP_006719679.1:n.16335+90A=
XM_011538770.1:c.16395+90A=	XP_011537072.1:n.16395+90A=
XM_011538771.1:c.16392+90A=	XP_011537073.1:n.16392+90A=
XM_011538772.1:c.16386+90A=	XP_011537074.1:n.16386+90A=
XM_011538773.1:c.16383+90A=	XP_011537075.1:n.16383+90A=
XM_011538774.1:c.16374+90A=	XP_011537076.1:n.16374+90A=
XM_011538775.1:c.16329+90A=	XP_011537077.1:n.16329+90A=
XM_011538776.1:c.16302+90A=	XP_011537078.1:n.16302+90A=
XM_005269162.4:c.16338+90A=	XP_005269219.1:n.16338+90A=
XM_006719614.4:c.16347+90A=	XP_006719677.1:n.16347+90A=
XM_006719616.3:c.16335+90A=	XP_006719679.1:n.16335+90A=
XM_011538770.2:c.16395+90A=	XP_011537072.1:n.16395+90A=
XM_011538771.2:c.16392+90A=	XP_011537073.1:n.16392+90A=
XM_011538772.2:c.16386+90A=	XP_011537074.1:n.16386+90A=
XM_011538773.2:c.16383+90A=	XP_011537075.1:n.16383+90A=
XM_011538774.2:c.16374+90A=	XP_011537076.1:n.16374+90A=
XM_011538776.2:c.16302+90A=	XP_011537078.1:n.16302+90A=
XR_001748874.1:n.16515+90A=
NM_003482.4:c.16338+90A= MANE Select	NP_003473.3:n.16338+90A=