Canonical Allele Identifier: CA2575144348

Gene: KMT2D

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49024728_49024729insTT , CM000674.2:g.49024728_49024729insTT	GRCh38
NC_000012.11:g.49418511_49418512insTT , CM000674.1:g.49418511_49418512insTT	GRCh37
NC_000012.10:g.47704778_47704779insTT	NCBI36
NG_027827.1:g.35597_35598insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681974.1:n.594-20_594-19insAA
ENST00000683543.2:c.15922-20_15922-19insAA	ENSP00000506726.1:n.15922-20_15922-19insAA
ENST00000683863.1:n.1637-20_1637-19insAA
ENST00000684428.1:c.457-20_457-19insAA	ENSP00000507433.1:n.457-20_457-19insAA
ENST00000684755.1:n.457-20_457-19insAA
ENST00000685024.1:c.1056_1057insAA
ENST00000685166.1:c.15931-20_15931-19insAA	ENSP00000509386.1:n.15931-20_15931-19insAA
ENST00000688411.1:c.399-20_399-19insAA	ENSP00000510146.1:n.399-20_399-19insAA
ENST00000692637.1:c.15919-20_15919-19insAA	ENSP00000509666.1:n.15919-20_15919-19insAA
ENST00000301067.12:c.15922-20_15922-19insAA MANE Select	ENSP00000301067.7:n.15922-20_15922-19insAA
ENST00000301067.11:c.15922-20_15922-19insAA	ENSP00000301067.7:n.15922-20_15922-19insAA
NM_003482.3:c.15922-20_15922-19insAA	NP_003473.3:n.15922-20_15922-19insAA
XM_005269162.3:c.15922-20_15922-19insAA	XP_005269219.1:n.15922-20_15922-19insAA
XM_006719614.2:c.15931-20_15931-19insAA	XP_006719677.1:n.15931-20_15931-19insAA
XM_006719616.2:c.15919-20_15919-19insAA	XP_006719679.1:n.15919-20_15919-19insAA
XM_011538770.1:c.15931-20_15931-19insAA	XP_011537072.1:n.15931-20_15931-19insAA
XM_011538771.1:c.15928-20_15928-19insAA	XP_011537073.1:n.15928-20_15928-19insAA
XM_011538772.1:c.15922-20_15922-19insAA	XP_011537074.1:n.15922-20_15922-19insAA
XM_011538773.1:c.15919-20_15919-19insAA	XP_011537075.1:n.15919-20_15919-19insAA
XM_011538774.1:c.15910-20_15910-19insAA	XP_011537076.1:n.15910-20_15910-19insAA
XM_011538775.1:c.15865-20_15865-19insAA	XP_011537077.1:n.15865-20_15865-19insAA
XM_011538776.1:c.15838-20_15838-19insAA	XP_011537078.1:n.15838-20_15838-19insAA
XR_944740.1:n.17110-20_17110-19insAA
XM_005269162.4:c.15922-20_15922-19insAA	XP_005269219.1:n.15922-20_15922-19insAA
XM_006719614.4:c.15931-20_15931-19insAA	XP_006719677.1:n.15931-20_15931-19insAA
XM_006719616.3:c.15919-20_15919-19insAA	XP_006719679.1:n.15919-20_15919-19insAA
XM_011538770.2:c.15931-20_15931-19insAA	XP_011537072.1:n.15931-20_15931-19insAA
XM_011538771.2:c.15928-20_15928-19insAA	XP_011537073.1:n.15928-20_15928-19insAA
XM_011538772.2:c.15922-20_15922-19insAA	XP_011537074.1:n.15922-20_15922-19insAA
XM_011538773.2:c.15919-20_15919-19insAA	XP_011537075.1:n.15919-20_15919-19insAA
XM_011538774.2:c.15910-20_15910-19insAA	XP_011537076.1:n.15910-20_15910-19insAA
XM_011538776.2:c.15838-20_15838-19insAA	XP_011537078.1:n.15838-20_15838-19insAA
XR_001748874.1:n.16099-20_16099-19insAA
NM_003482.4:c.15922-20_15922-19insAA MANE Select	NP_003473.3:n.15922-20_15922-19insAA