Canonical Allele Identifier: CA2571560795

Gene: KMT2D

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49022238_49022246del , CM000674.2:g.49022238_49022246del	GRCh38
NC_000012.11:g.49416021_49416029del , CM000674.1:g.49416021_49416029del	GRCh37
NC_000012.10:g.47702288_47702296del	NCBI36
NG_027827.1:g.38079_38087del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526209.2:c.382+34_382+42del
ENST00000681974.1:n.1084+34_1084+42del
ENST00000682693.1:n.2046+34_2046+42del
ENST00000682886.1:n.818+34_818+42del
ENST00000683543.2:c.16460+34_16460+42del	ENSP00000506726.1:n.16460+34_16460+42del
ENST00000683988.1:c.383+34_383+42del	ENSP00000506939.1:n.383+34_383+42del
ENST00000684428.1:c.1005+34_1005+42del	ENSP00000507433.1:n.1005+34_1005+42del
ENST00000685024.1:c.1566+34_1566+42del
ENST00000685166.1:c.16421+34_16421+42del	ENSP00000509386.1:n.16421+34_16421+42del
ENST00000691932.1:c.413+34_413+42del	ENSP00000509037.1:n.413+34_413+42del
ENST00000692637.1:c.16409+34_16409+42del	ENSP00000509666.1:n.16409+34_16409+42del
ENST00000301067.12:c.16412+34_16412+42del MANE Select	ENSP00000301067.7:n.16412+34_16412+42del
ENST00000301067.11:c.16412+34_16412+42del	ENSP00000301067.7:n.16412+34_16412+42del
ENST00000526209.1:c.455+34_455+42del	ENSP00000435714.1:n.455+34_455+42del
NM_003482.3:c.16412+34_16412+42del	NP_003473.3:n.16412+34_16412+42del
XM_005269162.3:c.16412+34_16412+42del	XP_005269219.1:n.16412+34_16412+42del
XM_006719614.2:c.16421+34_16421+42del	XP_006719677.1:n.16421+34_16421+42del
XM_006719616.2:c.16409+34_16409+42del	XP_006719679.1:n.16409+34_16409+42del
XM_011538770.1:c.16469+34_16469+42del	XP_011537072.1:n.16469+34_16469+42del
XM_011538771.1:c.16466+34_16466+42del	XP_011537073.1:n.16466+34_16466+42del
XM_011538772.1:c.16460+34_16460+42del	XP_011537074.1:n.16460+34_16460+42del
XM_011538773.1:c.16457+34_16457+42del	XP_011537075.1:n.16457+34_16457+42del
XM_011538774.1:c.16448+34_16448+42del	XP_011537076.1:n.16448+34_16448+42del
XM_011538775.1:c.16403+34_16403+42del	XP_011537077.1:n.16403+34_16403+42del
XM_011538776.1:c.16376+34_16376+42del	XP_011537078.1:n.16376+34_16376+42del
XM_005269162.4:c.16412+34_16412+42del	XP_005269219.1:n.16412+34_16412+42del
XM_006719614.4:c.16421+34_16421+42del	XP_006719677.1:n.16421+34_16421+42del
XM_006719616.3:c.16409+34_16409+42del	XP_006719679.1:n.16409+34_16409+42del
XM_011538770.2:c.16469+34_16469+42del	XP_011537072.1:n.16469+34_16469+42del
XM_011538771.2:c.16466+34_16466+42del	XP_011537073.1:n.16466+34_16466+42del
XM_011538772.2:c.16460+34_16460+42del	XP_011537074.1:n.16460+34_16460+42del
XM_011538773.2:c.16457+34_16457+42del	XP_011537075.1:n.16457+34_16457+42del
XM_011538774.2:c.16448+34_16448+42del	XP_011537076.1:n.16448+34_16448+42del
XM_011538776.2:c.16376+34_16376+42del	XP_011537078.1:n.16376+34_16376+42del
XR_001748874.1:n.16589+34_16589+42del
NM_003482.4:c.16412+34_16412+42del MANE Select	NP_003473.3:n.16412+34_16412+42del