Canonical Allele Identifier: CA2034963026
Gene: KMT2D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49022136G= , CM000674.2:g.49022136G= GRCh38
NC_000012.11:g.49415919G= , CM000674.1:g.49415919G= GRCh37
NC_000012.10:g.47702186G= NCBI36
NG_027827.1:g.38189C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000526209.2:c.398C=
ENST00000681974.1:n.1100C=
ENST00000682693.1:n.2062C=
ENST00000682886.1:n.834C=
ENST00000683543.2:c.16476C= ENSP00000506726.1:p.Ser5492=
ENST00000683988.1:c.399C= ENSP00000506939.1:p.Ser133=
ENST00000684428.1:c.1021C= ENSP00000507433.1:n.1021C=
ENST00000685024.1:c.1582C=
ENST00000685166.1:c.16437C= ENSP00000509386.1:p.Ser5479=
ENST00000691932.1:c.429C= ENSP00000509037.1:p.Ser143=
ENST00000692637.1:c.16425C= ENSP00000509666.1:p.Ser5475=
ENST00000301067.12:c.16428C= MANE Select ENSP00000301067.7:p.Ser5476=
ENST00000301067.11:c.16428C= ENSP00000301067.7:p.Ser5476=
ENST00000526209.1:c.471C= ENSP00000435714.1:p.Ser157=
NM_003482.3:c.16428C= NP_003473.3:p.Ser5476=
XM_005269162.3:c.16428C= XP_005269219.1:p.Ser5476=
XM_006719614.2:c.16437C= XP_006719677.1:p.Ser5479=
XM_006719616.2:c.16425C= XP_006719679.1:p.Ser5475=
XM_011538770.1:c.16485C= XP_011537072.1:p.Ser5495=
XM_011538771.1:c.16482C= XP_011537073.1:p.Ser5494=
XM_011538772.1:c.16476C= XP_011537074.1:p.Ser5492=
XM_011538773.1:c.16473C= XP_011537075.1:p.Ser5491=
XM_011538774.1:c.16464C= XP_011537076.1:p.Ser5488=
XM_011538775.1:c.16419C= XP_011537077.1:p.Ser5473=
XM_011538776.1:c.16392C= XP_011537078.1:p.Ser5464=
XM_005269162.4:c.16428C= XP_005269219.1:p.Ser5476=
XM_006719614.4:c.16437C= XP_006719677.1:p.Ser5479=
XM_006719616.3:c.16425C= XP_006719679.1:p.Ser5475=
XM_011538770.2:c.16485C= XP_011537072.1:p.Ser5495=
XM_011538771.2:c.16482C= XP_011537073.1:p.Ser5494=
XM_011538772.2:c.16476C= XP_011537074.1:p.Ser5492=
XM_011538773.2:c.16473C= XP_011537075.1:p.Ser5491=
XM_011538774.2:c.16464C= XP_011537076.1:p.Ser5488=
XM_011538776.2:c.16392C= XP_011537078.1:p.Ser5464=
XR_001748874.1:n.16605C=
NM_003482.4:c.16428C= MANE Select NP_003473.3:p.Ser5476=