Canonical Allele Identifier: CA2034963110

Gene: KMT2D

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49022263_49022265delinsTCC , CM000674.2:g.49022263_49022265delinsTCC	GRCh38
NC_000012.11:g.49416046_49416048delinsTCC , CM000674.1:g.49416046_49416048delinsTCC	GRCh37
NC_000012.10:g.47702313_47702315delinsTCC	NCBI36
NG_027827.1:g.38060_38062delinsGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526209.2:c.382+15_382+17delinsGGA
ENST00000681974.1:n.1084+15_1084+17delinsGGA
ENST00000682693.1:n.2046+15_2046+17delinsGGA
ENST00000682886.1:n.818+15_818+17delinsGGA
ENST00000683543.2:c.16460+15_16460+17delinsGGA	ENSP00000506726.1:n.16460+15_16460+17delinsGGA
ENST00000683988.1:c.383+15_383+17delinsGGA	ENSP00000506939.1:n.383+15_383+17delinsGGA
ENST00000684428.1:c.1005+15_1005+17delinsGGA	ENSP00000507433.1:n.1005+15_1005+17delinsGGA
ENST00000685024.1:c.1566+15_1566+17delinsGGA
ENST00000685166.1:c.16421+15_16421+17delinsGGA	ENSP00000509386.1:n.16421+15_16421+17delinsGGA
ENST00000691932.1:c.413+15_413+17delinsGGA	ENSP00000509037.1:n.413+15_413+17delinsGGA
ENST00000692637.1:c.16409+15_16409+17delinsGGA	ENSP00000509666.1:n.16409+15_16409+17delinsGGA
ENST00000301067.12:c.16412+15_16412+17delinsGGA MANE Select	ENSP00000301067.7:n.16412+15_16412+17delinsGGA
ENST00000301067.11:c.16412+15_16412+17delinsGGA	ENSP00000301067.7:n.16412+15_16412+17delinsGGA
ENST00000526209.1:c.455+15_455+17delinsGGA	ENSP00000435714.1:n.455+15_455+17delinsGGA
NM_003482.3:c.16412+15_16412+17delinsGGA	NP_003473.3:n.16412+15_16412+17delinsGGA
XM_005269162.3:c.16412+15_16412+17delinsGGA	XP_005269219.1:n.16412+15_16412+17delinsGGA
XM_006719614.2:c.16421+15_16421+17delinsGGA	XP_006719677.1:n.16421+15_16421+17delinsGGA
XM_006719616.2:c.16409+15_16409+17delinsGGA	XP_006719679.1:n.16409+15_16409+17delinsGGA
XM_011538770.1:c.16469+15_16469+17delinsGGA	XP_011537072.1:n.16469+15_16469+17delinsGGA
XM_011538771.1:c.16466+15_16466+17delinsGGA	XP_011537073.1:n.16466+15_16466+17delinsGGA
XM_011538772.1:c.16460+15_16460+17delinsGGA	XP_011537074.1:n.16460+15_16460+17delinsGGA
XM_011538773.1:c.16457+15_16457+17delinsGGA	XP_011537075.1:n.16457+15_16457+17delinsGGA
XM_011538774.1:c.16448+15_16448+17delinsGGA	XP_011537076.1:n.16448+15_16448+17delinsGGA
XM_011538775.1:c.16403+15_16403+17delinsGGA	XP_011537077.1:n.16403+15_16403+17delinsGGA
XM_011538776.1:c.16376+15_16376+17delinsGGA	XP_011537078.1:n.16376+15_16376+17delinsGGA
XM_005269162.4:c.16412+15_16412+17delinsGGA	XP_005269219.1:n.16412+15_16412+17delinsGGA
XM_006719614.4:c.16421+15_16421+17delinsGGA	XP_006719677.1:n.16421+15_16421+17delinsGGA
XM_006719616.3:c.16409+15_16409+17delinsGGA	XP_006719679.1:n.16409+15_16409+17delinsGGA
XM_011538770.2:c.16469+15_16469+17delinsGGA	XP_011537072.1:n.16469+15_16469+17delinsGGA
XM_011538771.2:c.16466+15_16466+17delinsGGA	XP_011537073.1:n.16466+15_16466+17delinsGGA
XM_011538772.2:c.16460+15_16460+17delinsGGA	XP_011537074.1:n.16460+15_16460+17delinsGGA
XM_011538773.2:c.16457+15_16457+17delinsGGA	XP_011537075.1:n.16457+15_16457+17delinsGGA
XM_011538774.2:c.16448+15_16448+17delinsGGA	XP_011537076.1:n.16448+15_16448+17delinsGGA
XM_011538776.2:c.16376+15_16376+17delinsGGA	XP_011537078.1:n.16376+15_16376+17delinsGGA
XR_001748874.1:n.16589+15_16589+17delinsGGA
NM_003482.4:c.16412+15_16412+17delinsGGA MANE Select	NP_003473.3:n.16412+15_16412+17delinsGGA