Canonical Allele Identifier: CA2034964115

Gene: KMT2D

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49024727C= , CM000674.2:g.49024727C=	GRCh38
NC_000012.11:g.49418510C= , CM000674.1:g.49418510C=	GRCh37
NC_000012.10:g.47704777C=	NCBI36
NG_027827.1:g.35598G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681974.1:n.594-19G=
ENST00000683543.2:c.15922-19G=	ENSP00000506726.1:n.15922-19G=
ENST00000683863.1:n.1637-19G=
ENST00000684428.1:c.457-19G=	ENSP00000507433.1:n.457-19G=
ENST00000684755.1:n.457-19G=
ENST00000685024.1:c.1057G=
ENST00000685166.1:c.15931-19G=	ENSP00000509386.1:n.15931-19G=
ENST00000688411.1:c.399-19G=	ENSP00000510146.1:n.399-19G=
ENST00000692637.1:c.15919-19G=	ENSP00000509666.1:n.15919-19G=
ENST00000301067.12:c.15922-19G= MANE Select	ENSP00000301067.7:n.15922-19G=
ENST00000301067.11:c.15922-19G=	ENSP00000301067.7:n.15922-19G=
NM_003482.3:c.15922-19G=	NP_003473.3:n.15922-19G=
XM_005269162.3:c.15922-19G=	XP_005269219.1:n.15922-19G=
XM_006719614.2:c.15931-19G=	XP_006719677.1:n.15931-19G=
XM_006719616.2:c.15919-19G=	XP_006719679.1:n.15919-19G=
XM_011538770.1:c.15931-19G=	XP_011537072.1:n.15931-19G=
XM_011538771.1:c.15928-19G=	XP_011537073.1:n.15928-19G=
XM_011538772.1:c.15922-19G=	XP_011537074.1:n.15922-19G=
XM_011538773.1:c.15919-19G=	XP_011537075.1:n.15919-19G=
XM_011538774.1:c.15910-19G=	XP_011537076.1:n.15910-19G=
XM_011538775.1:c.15865-19G=	XP_011537077.1:n.15865-19G=
XM_011538776.1:c.15838-19G=	XP_011537078.1:n.15838-19G=
XR_944740.1:n.17110-19G=
XM_005269162.4:c.15922-19G=	XP_005269219.1:n.15922-19G=
XM_006719614.4:c.15931-19G=	XP_006719677.1:n.15931-19G=
XM_006719616.3:c.15919-19G=	XP_006719679.1:n.15919-19G=
XM_011538770.2:c.15931-19G=	XP_011537072.1:n.15931-19G=
XM_011538771.2:c.15928-19G=	XP_011537073.1:n.15928-19G=
XM_011538772.2:c.15922-19G=	XP_011537074.1:n.15922-19G=
XM_011538773.2:c.15919-19G=	XP_011537075.1:n.15919-19G=
XM_011538774.2:c.15910-19G=	XP_011537076.1:n.15910-19G=
XM_011538776.2:c.15838-19G=	XP_011537078.1:n.15838-19G=
XR_001748874.1:n.16099-19G=
NM_003482.4:c.15922-19G= MANE Select	NP_003473.3:n.15922-19G=