Canonical Allele Identifier: CA6545919
Community Standard Title: NM_003482.4(KMT2D):c.13710C>T (p.Thr4570=)
Gene: KMT2D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49030730G>A , CM000674.2:g.49030730G>A GRCh38
NC_000012.11:g.49424513G>A , CM000674.1:g.49424513G>A GRCh37
NC_000012.10:g.47710780G>A NCBI36
NG_027827.1:g.29595C>T

Transcript Alleles

HGVS Amino-acid Change
NM_003482.4:c.13710C>T MANE Select NP_003473.3:p.Thr4570=
ENST00000301067.12:c.13710C>T MANE Select ENSP00000301067.7:p.Thr4570=
NM_003482.3:c.13710C>T NP_003473.3:p.Thr4570=
ENST00000301067.11:c.13710C>T ENSP00000301067.7:p.Thr4570=
ENST00000552391.1:n.410C>T
ENST00000552391.2:n.410C>T
ENST00000683543.2:c.13710C>T ENSP00000506726.1:p.Thr4570=
ENST00000685166.1:c.13719C>T ENSP00000509386.1:p.Thr4573=
ENST00000685979.1:c.39C>T ENSP00000508906.1:p.Thr13=
ENST00000685982.1:c.177C>T ENSP00000508613.1:p.Thr59=
ENST00000686564.1:c.39C>T ENSP00000509290.1:p.Thr13=
ENST00000691986.1:c.139-291C>T ENSP00000509196.1:n.139-291C>T
ENST00000692637.1:c.13707C>T ENSP00000509666.1:p.Thr4569=
ENST00000692973.1:c.311C>T ENSP00000508893.1:n.311C>T
XM_005269162.3:c.13710C>T XP_005269219.1:p.Thr4570=
XM_005269162.4:c.13710C>T XP_005269219.1:p.Thr4570=
XM_006719614.2:c.13719C>T XP_006719677.1:p.Thr4573=
XM_006719614.4:c.13719C>T XP_006719677.1:p.Thr4573=
XM_006719616.2:c.13707C>T XP_006719679.1:p.Thr4569=
XM_006719616.3:c.13707C>T XP_006719679.1:p.Thr4569=
XM_011538770.1:c.13719C>T XP_011537072.1:p.Thr4573=
XM_011538770.2:c.13719C>T XP_011537072.1:p.Thr4573=
XM_011538771.1:c.13716C>T XP_011537073.1:p.Thr4572=
XM_011538771.2:c.13716C>T XP_011537073.1:p.Thr4572=
XM_011538772.1:c.13710C>T XP_011537074.1:p.Thr4570=
XM_011538772.2:c.13710C>T XP_011537074.1:p.Thr4570=
XM_011538773.1:c.13707C>T XP_011537075.1:p.Thr4569=
XM_011538773.2:c.13707C>T XP_011537075.1:p.Thr4569=
XM_011538774.1:c.13698C>T XP_011537076.1:p.Thr4566=
XM_011538774.2:c.13698C>T XP_011537076.1:p.Thr4566=
XM_011538775.1:c.13719C>T XP_011537077.1:p.Thr4573=
XM_011538776.1:c.13626C>T XP_011537078.1:p.Thr4542=
XM_011538776.2:c.13626C>T XP_011537078.1:p.Thr4542=
XR_001748874.1:n.15028C>T
XR_944740.1:n.16039C>T