Canonical Allele Identifier: CA2034963162
Gene: KMT2D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49022325T= , CM000674.2:g.49022325T= GRCh38
NC_000012.11:g.49416108T= , CM000674.1:g.49416108T= GRCh37
NC_000012.10:g.47702375T= NCBI36
NG_027827.1:g.38000A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000526209.2:c.337A=
ENST00000681974.1:n.1039A=
ENST00000682693.1:n.2001A=
ENST00000682886.1:n.773A=
ENST00000683543.2:c.16415A= ENSP00000506726.1:p.Asn5472=
ENST00000683988.1:c.338A= ENSP00000506939.1:p.Asn113=
ENST00000684428.1:c.960A= ENSP00000507433.1:p.Lys320=
ENST00000685024.1:c.1521A=
ENST00000685166.1:c.16376A= ENSP00000509386.1:p.Asn5459=
ENST00000691932.1:c.368A= ENSP00000509037.1:p.Asn123=
ENST00000692637.1:c.16364A= ENSP00000509666.1:p.Asn5455=
ENST00000301067.12:c.16367A= MANE Select ENSP00000301067.7:p.Asn5456=
ENST00000301067.11:c.16367A= ENSP00000301067.7:p.Asn5456=
ENST00000526209.1:c.410A= ENSP00000435714.1:p.Asn137=
NM_003482.3:c.16367A= NP_003473.3:p.Asn5456=
XM_005269162.3:c.16367A= XP_005269219.1:p.Asn5456=
XM_006719614.2:c.16376A= XP_006719677.1:p.Asn5459=
XM_006719616.2:c.16364A= XP_006719679.1:p.Asn5455=
XM_011538770.1:c.16424A= XP_011537072.1:p.Asn5475=
XM_011538771.1:c.16421A= XP_011537073.1:p.Asn5474=
XM_011538772.1:c.16415A= XP_011537074.1:p.Asn5472=
XM_011538773.1:c.16412A= XP_011537075.1:p.Asn5471=
XM_011538774.1:c.16403A= XP_011537076.1:p.Asn5468=
XM_011538775.1:c.16358A= XP_011537077.1:p.Asn5453=
XM_011538776.1:c.16331A= XP_011537078.1:p.Asn5444=
XM_005269162.4:c.16367A= XP_005269219.1:p.Asn5456=
XM_006719614.4:c.16376A= XP_006719677.1:p.Asn5459=
XM_006719616.3:c.16364A= XP_006719679.1:p.Asn5455=
XM_011538770.2:c.16424A= XP_011537072.1:p.Asn5475=
XM_011538771.2:c.16421A= XP_011537073.1:p.Asn5474=
XM_011538772.2:c.16415A= XP_011537074.1:p.Asn5472=
XM_011538773.2:c.16412A= XP_011537075.1:p.Asn5471=
XM_011538774.2:c.16403A= XP_011537076.1:p.Asn5468=
XM_011538776.2:c.16331A= XP_011537078.1:p.Asn5444=
XR_001748874.1:n.16544A=
NM_003482.4:c.16367A= MANE Select NP_003473.3:p.Asn5456=