Canonical Allele Identifier: CA2726328078

Gene: KMT2D

Linked Data

• dbSNP Id: rs2137710395

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49024544_49024549del , CM000674.2:g.49024544_49024549del	GRCh38
NC_000012.11:g.49418327_49418332del , CM000674.1:g.49418327_49418332del	GRCh37
NC_000012.10:g.47704594_47704599del	NCBI36
NG_027827.1:g.35785_35790del

Transcript Alleles

HGVS	Amino-acid change
ENST00000681974.1:n.724+38_724+43del
ENST00000682693.1:n.22_27del
ENST00000683543.2:c.16052+38_16052+43del	ENSP00000506726.1:n.16052+38_16052+43del
ENST00000683863.1:n.1805_1810del
ENST00000684428.1:c.587+38_587+43del	ENSP00000507433.1:n.587+38_587+43del
ENST00000684755.1:n.587+38_587+43del
ENST00000685024.1:c.1206+38_1206+43del
ENST00000685166.1:c.16061+38_16061+43del	ENSP00000509386.1:n.16061+38_16061+43del
ENST00000688411.1:c.529+38_529+43del	ENSP00000510146.1:n.529+38_529+43del
ENST00000691932.1:c.131+38_131+43del	ENSP00000509037.1:n.131+38_131+43del
ENST00000692637.1:c.16049+38_16049+43del	ENSP00000509666.1:n.16049+38_16049+43del
ENST00000301067.12:c.16052+38_16052+43del MANE Select	ENSP00000301067.7:n.16052+38_16052+43del
ENST00000301067.11:c.16052+38_16052+43del	ENSP00000301067.7:n.16052+38_16052+43del
ENST00000526209.1:c.47+38_47+43del	ENSP00000435714.1:n.47+38_47+43del
NM_003482.3:c.16052+38_16052+43del	NP_003473.3:n.16052+38_16052+43del
XM_005269162.3:c.16052+38_16052+43del	XP_005269219.1:n.16052+38_16052+43del
XM_006719614.2:c.16061+38_16061+43del	XP_006719677.1:n.16061+38_16061+43del
XM_006719616.2:c.16049+38_16049+43del	XP_006719679.1:n.16049+38_16049+43del
XM_011538770.1:c.16061+38_16061+43del	XP_011537072.1:n.16061+38_16061+43del
XM_011538771.1:c.16058+38_16058+43del	XP_011537073.1:n.16058+38_16058+43del
XM_011538772.1:c.16052+38_16052+43del	XP_011537074.1:n.16052+38_16052+43del
XM_011538773.1:c.16049+38_16049+43del	XP_011537075.1:n.16049+38_16049+43del
XM_011538774.1:c.16040+38_16040+43del	XP_011537076.1:n.16040+38_16040+43del
XM_011538775.1:c.15995+38_15995+43del	XP_011537077.1:n.15995+38_15995+43del
XM_011538776.1:c.15968+38_15968+43del	XP_011537078.1:n.15968+38_15968+43del
XM_005269162.4:c.16052+38_16052+43del	XP_005269219.1:n.16052+38_16052+43del
XM_006719614.4:c.16061+38_16061+43del	XP_006719677.1:n.16061+38_16061+43del
XM_006719616.3:c.16049+38_16049+43del	XP_006719679.1:n.16049+38_16049+43del
XM_011538770.2:c.16061+38_16061+43del	XP_011537072.1:n.16061+38_16061+43del
XM_011538771.2:c.16058+38_16058+43del	XP_011537073.1:n.16058+38_16058+43del
XM_011538772.2:c.16052+38_16052+43del	XP_011537074.1:n.16052+38_16052+43del
XM_011538773.2:c.16049+38_16049+43del	XP_011537075.1:n.16049+38_16049+43del
XM_011538774.2:c.16040+38_16040+43del	XP_011537076.1:n.16040+38_16040+43del
XM_011538776.2:c.15968+38_15968+43del	XP_011537078.1:n.15968+38_15968+43del
XR_001748874.1:n.16229+38_16229+43del
NM_003482.4:c.16052+38_16052+43del MANE Select	NP_003473.3:n.16052+38_16052+43del