Canonical Allele Identifier: CA2034945920
Gene: KMT2D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49031722G= , CM000674.2:g.49031722G= GRCh38
NC_000012.11:g.49425505G= , CM000674.1:g.49425505G= GRCh37
NC_000012.10:g.47711772G= NCBI36
NG_027827.1:g.28603C=

Transcript Alleles

HGVS Amino-acid change
ENST00000683543.2:c.12983C= ENSP00000506726.1:p.Ser4328=
ENST00000685166.1:c.12992C= ENSP00000509386.1:p.Ser4331=
ENST00000685554.1:c.1753-410C= ENSP00000508640.1:n.1753-410C=
ENST00000692637.1:c.12980C= ENSP00000509666.1:p.Ser4327=
ENST00000692841.1:c.4462C= ENSP00000508711.1:n.4462C=
ENST00000301067.12:c.12983C= MANE Select ENSP00000301067.7:p.Ser4328=
ENST00000301067.11:c.12983C= ENSP00000301067.7:p.Ser4328=
NM_003482.3:c.12983C= NP_003473.3:p.Ser4328=
XM_005269162.3:c.12983C= XP_005269219.1:p.Ser4328=
XM_006719614.2:c.12992C= XP_006719677.1:p.Ser4331=
XM_006719616.2:c.12980C= XP_006719679.1:p.Ser4327=
XM_011538770.1:c.12992C= XP_011537072.1:p.Ser4331=
XM_011538771.1:c.12989C= XP_011537073.1:p.Ser4330=
XM_011538772.1:c.12983C= XP_011537074.1:p.Ser4328=
XM_011538773.1:c.12980C= XP_011537075.1:p.Ser4327=
XM_011538774.1:c.12971C= XP_011537076.1:p.Ser4324=
XM_011538775.1:c.12992C= XP_011537077.1:p.Ser4331=
XM_011538776.1:c.12899C= XP_011537078.1:p.Ser4300=
XR_944740.1:n.15312C=
XM_005269162.4:c.12983C= XP_005269219.1:p.Ser4328=
XM_006719614.4:c.12992C= XP_006719677.1:p.Ser4331=
XM_006719616.3:c.12980C= XP_006719679.1:p.Ser4327=
XM_011538770.2:c.12992C= XP_011537072.1:p.Ser4331=
XM_011538771.2:c.12989C= XP_011537073.1:p.Ser4330=
XM_011538772.2:c.12983C= XP_011537074.1:p.Ser4328=
XM_011538773.2:c.12980C= XP_011537075.1:p.Ser4327=
XM_011538774.2:c.12971C= XP_011537076.1:p.Ser4324=
XM_011538776.2:c.12899C= XP_011537078.1:p.Ser4300=
XR_001748874.1:n.14301C=
NM_003482.4:c.12983C= MANE Select NP_003473.3:p.Ser4328=