Canonical Allele Identifier: CA236612640
Gene: KMT2D HGNC NCBI

Linked Data

dbSNP Id: rs527934291

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49042564G>A , CM000674.2:g.49042564G>A GRCh38
NC_000012.11:g.49436347G>A , CM000674.1:g.49436347G>A GRCh37
NC_000012.10:g.47722614G>A NCBI36
NG_027827.1:g.17761C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650290.2:c.676C>T
ENST00000683543.2:c.5864C>T ENSP00000506726.1:p.Ser1955Phe
ENST00000685166.1:c.5873C>T ENSP00000509386.1:p.Ser1958Phe
ENST00000688095.1:c.1813C>T ENSP00000510007.1:n.1813C>T
ENST00000692637.1:c.5861C>T ENSP00000509666.1:p.Ser1954Phe
ENST00000301067.12:c.5864C>T MANE Select ENSP00000301067.7:p.Ser1955Phe
ENST00000301067.11:c.5864C>T ENSP00000301067.7:p.Ser1955Phe
NM_003482.3:c.5864C>T NP_003473.3:p.Ser1955Phe
XM_005269162.3:c.5864C>T XP_005269219.1:p.Ser1955Phe
XM_006719614.2:c.5873C>T XP_006719677.1:p.Ser1958Phe
XM_006719616.2:c.5861C>T XP_006719679.1:p.Ser1954Phe
XM_011538770.1:c.5873C>T XP_011537072.1:p.Ser1958Phe
XM_011538771.1:c.5870C>T XP_011537073.1:p.Ser1957Phe
XM_011538772.1:c.5864C>T XP_011537074.1:p.Ser1955Phe
XM_011538773.1:c.5861C>T XP_011537075.1:p.Ser1954Phe
XM_011538774.1:c.5873C>T XP_011537076.1:p.Ser1958Phe
XM_011538775.1:c.5873C>T XP_011537077.1:p.Ser1958Phe
XM_011538776.1:c.5873C>T XP_011537078.1:p.Ser1958Phe
XR_944740.1:n.8193C>T
XM_005269162.4:c.5864C>T XP_005269219.1:p.Ser1955Phe
XM_006719614.4:c.5873C>T XP_006719677.1:p.Ser1958Phe
XM_006719616.3:c.5861C>T XP_006719679.1:p.Ser1954Phe
XM_011538770.2:c.5873C>T XP_011537072.1:p.Ser1958Phe
XM_011538771.2:c.5870C>T XP_011537073.1:p.Ser1957Phe
XM_011538772.2:c.5864C>T XP_011537074.1:p.Ser1955Phe
XM_011538773.2:c.5861C>T XP_011537075.1:p.Ser1954Phe
XM_011538774.2:c.5873C>T XP_011537076.1:p.Ser1958Phe
XM_011538776.2:c.5873C>T XP_011537078.1:p.Ser1958Phe
XR_001748874.1:n.7182C>T
NM_003482.4:c.5864C>T MANE Select NP_003473.3:p.Ser1955Phe