Canonical Allele Identifier: CA384703452
Gene: KMT2D HGNC NCBI

Linked Data

dbSNP Id: rs2120412454

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49030963C>A , CM000674.2:g.49030963C>A GRCh38
NC_000012.11:g.49424746C>A , CM000674.1:g.49424746C>A GRCh37
NC_000012.10:g.47711013C>A NCBI36
NG_027827.1:g.29362G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000552391.2:n.301G>T
ENST00000683543.2:c.13601G>T ENSP00000506726.1:p.Ser4534Ile
ENST00000685166.1:c.13610G>T ENSP00000509386.1:p.Ser4537Ile
ENST00000685982.1:c.139-195G>T ENSP00000508613.1:n.139-195G>T
ENST00000691986.1:c.138+212G>T ENSP00000509196.1:n.138+212G>T
ENST00000692637.1:c.13598G>T ENSP00000509666.1:p.Ser4533Ile
ENST00000692973.1:c.202G>T ENSP00000508893.1:n.202G>T
ENST00000301067.12:c.13601G>T MANE Select ENSP00000301067.7:p.Ser4534Ile
ENST00000301067.11:c.13601G>T ENSP00000301067.7:p.Ser4534Ile
ENST00000552391.1:n.301G>T
NM_003482.3:c.13601G>T NP_003473.3:p.Ser4534Ile
XM_005269162.3:c.13601G>T XP_005269219.1:p.Ser4534Ile
XM_006719614.2:c.13610G>T XP_006719677.1:p.Ser4537Ile
XM_006719616.2:c.13598G>T XP_006719679.1:p.Ser4533Ile
XM_011538770.1:c.13610G>T XP_011537072.1:p.Ser4537Ile
XM_011538771.1:c.13607G>T XP_011537073.1:p.Ser4536Ile
XM_011538772.1:c.13601G>T XP_011537074.1:p.Ser4534Ile
XM_011538773.1:c.13598G>T XP_011537075.1:p.Ser4533Ile
XM_011538774.1:c.13589G>T XP_011537076.1:p.Ser4530Ile
XM_011538775.1:c.13610G>T XP_011537077.1:p.Ser4537Ile
XM_011538776.1:c.13517G>T XP_011537078.1:p.Ser4506Ile
XR_944740.1:n.15930G>T
XM_005269162.4:c.13601G>T XP_005269219.1:p.Ser4534Ile
XM_006719614.4:c.13610G>T XP_006719677.1:p.Ser4537Ile
XM_006719616.3:c.13598G>T XP_006719679.1:p.Ser4533Ile
XM_011538770.2:c.13610G>T XP_011537072.1:p.Ser4537Ile
XM_011538771.2:c.13607G>T XP_011537073.1:p.Ser4536Ile
XM_011538772.2:c.13601G>T XP_011537074.1:p.Ser4534Ile
XM_011538773.2:c.13598G>T XP_011537075.1:p.Ser4533Ile
XM_011538774.2:c.13589G>T XP_011537076.1:p.Ser4530Ile
XM_011538776.2:c.13517G>T XP_011537078.1:p.Ser4506Ile
XR_001748874.1:n.14919G>T
NM_003482.4:c.13601G>T MANE Select NP_003473.3:p.Ser4534Ile