Canonical Allele Identifier: CA2034964126

Gene: KMT2D

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49024742_49024743delinsGT , CM000674.2:g.49024742_49024743delinsGT	GRCh38
NC_000012.11:g.49418525_49418526delinsGT , CM000674.1:g.49418525_49418526delinsGT	GRCh37
NC_000012.10:g.47704792_47704793delinsGT	NCBI36
NG_027827.1:g.35582_35583delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681974.1:n.594-35_594-34delinsAC
ENST00000683543.2:c.15922-35_15922-34delinsAC	ENSP00000506726.1:n.15922-35_15922-34delinsAC
ENST00000683863.1:n.1637-35_1637-34delinsAC
ENST00000684428.1:c.457-35_457-34delinsAC	ENSP00000507433.1:n.457-35_457-34delinsAC
ENST00000684755.1:n.457-35_457-34delinsAC
ENST00000685024.1:c.1047-6_1047-5delinsAC
ENST00000685166.1:c.15931-35_15931-34delinsAC	ENSP00000509386.1:n.15931-35_15931-34delinsAC
ENST00000688411.1:c.399-35_399-34delinsAC	ENSP00000510146.1:n.399-35_399-34delinsAC
ENST00000692637.1:c.15919-35_15919-34delinsAC	ENSP00000509666.1:n.15919-35_15919-34delinsAC
ENST00000301067.12:c.15922-35_15922-34delinsAC MANE Select	ENSP00000301067.7:n.15922-35_15922-34delinsAC
ENST00000301067.11:c.15922-35_15922-34delinsAC	ENSP00000301067.7:n.15922-35_15922-34delinsAC
NM_003482.3:c.15922-35_15922-34delinsAC	NP_003473.3:n.15922-35_15922-34delinsAC
XM_005269162.3:c.15922-35_15922-34delinsAC	XP_005269219.1:n.15922-35_15922-34delinsAC
XM_006719614.2:c.15931-35_15931-34delinsAC	XP_006719677.1:n.15931-35_15931-34delinsAC
XM_006719616.2:c.15919-35_15919-34delinsAC	XP_006719679.1:n.15919-35_15919-34delinsAC
XM_011538770.1:c.15931-35_15931-34delinsAC	XP_011537072.1:n.15931-35_15931-34delinsAC
XM_011538771.1:c.15928-35_15928-34delinsAC	XP_011537073.1:n.15928-35_15928-34delinsAC
XM_011538772.1:c.15922-35_15922-34delinsAC	XP_011537074.1:n.15922-35_15922-34delinsAC
XM_011538773.1:c.15919-35_15919-34delinsAC	XP_011537075.1:n.15919-35_15919-34delinsAC
XM_011538774.1:c.15910-35_15910-34delinsAC	XP_011537076.1:n.15910-35_15910-34delinsAC
XM_011538775.1:c.15865-35_15865-34delinsAC	XP_011537077.1:n.15865-35_15865-34delinsAC
XM_011538776.1:c.15838-35_15838-34delinsAC	XP_011537078.1:n.15838-35_15838-34delinsAC
XR_944740.1:n.17110-35_17110-34delinsAC
XM_005269162.4:c.15922-35_15922-34delinsAC	XP_005269219.1:n.15922-35_15922-34delinsAC
XM_006719614.4:c.15931-35_15931-34delinsAC	XP_006719677.1:n.15931-35_15931-34delinsAC
XM_006719616.3:c.15919-35_15919-34delinsAC	XP_006719679.1:n.15919-35_15919-34delinsAC
XM_011538770.2:c.15931-35_15931-34delinsAC	XP_011537072.1:n.15931-35_15931-34delinsAC
XM_011538771.2:c.15928-35_15928-34delinsAC	XP_011537073.1:n.15928-35_15928-34delinsAC
XM_011538772.2:c.15922-35_15922-34delinsAC	XP_011537074.1:n.15922-35_15922-34delinsAC
XM_011538773.2:c.15919-35_15919-34delinsAC	XP_011537075.1:n.15919-35_15919-34delinsAC
XM_011538774.2:c.15910-35_15910-34delinsAC	XP_011537076.1:n.15910-35_15910-34delinsAC
XM_011538776.2:c.15838-35_15838-34delinsAC	XP_011537078.1:n.15838-35_15838-34delinsAC
XR_001748874.1:n.16099-35_16099-34delinsAC
NM_003482.4:c.15922-35_15922-34delinsAC MANE Select	NP_003473.3:n.15922-35_15922-34delinsAC