Canonical Allele Identifier: CA1980500644
Gene: KMT5B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68158179G= , CM000673.2:g.68158179G= GRCh38
NC_000011.9:g.67925646G= , CM000673.1:g.67925646G= GRCh37
NC_000011.8:g.67682222G= NCBI36
NG_052873.1:g.60594C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453170.6:c.1954C= ENSP00000406377.2:p.Arg652=
ENST00000524672.3:n.2519C=
ENST00000700520.1:c.*1791C= ENSP00000515027.1:n.*1791C=
ENST00000700521.1:c.*1834C= ENSP00000515028.1:n.*1834C=
ENST00000700522.1:c.*1834C= ENSP00000515029.1:n.*1834C=
ENST00000700523.1:c.1651C= ENSP00000515030.1:p.Arg551=
ENST00000700524.1:c.*1375C= ENSP00000515031.1:n.*1375C=
ENST00000304363.9:c.2167C= MANE Select ENSP00000305899.4:p.Arg723=
ENST00000304363.8:c.2167C= ENSP00000305899.4:p.Arg723=
ENST00000441488.6:c.*1375C= ENSP00000411146.2:n.*1375C=
ENST00000615954.4:c.2167C= ENSP00000484858.1:p.Arg723=
NM_001300907.1:c.1651C= NP_001287836.1:p.Arg551=
NM_001300908.1:c.1447C= NP_001287837.1:p.Arg483=
NM_017635.4:c.2167C= NP_060105.3:p.Arg723=
XM_005274035.2:c.2167C= XP_005274092.2:p.Arg723=
XM_005274036.2:c.2098C= XP_005274093.2:p.Arg700=
XM_005274037.1:c.1651C= XP_005274094.1:p.Arg551=
XM_006718581.1:c.2098C= XP_006718644.1:p.Arg700=
XM_011545091.1:c.2167C= XP_011543393.1:p.Arg723=
XM_011545092.1:c.1954C= XP_011543394.1:p.Arg652=
XM_011545093.1:c.925C= XP_011543395.1:p.Arg309=
XM_005274035.4:c.2167C= XP_005274092.2:p.Arg723=
XM_005274036.4:c.2098C= XP_005274093.2:p.Arg700=
XM_006718581.2:c.2098C= XP_006718644.1:p.Arg700=
XM_011545092.3:c.1954C= XP_011543394.1:p.Arg652=
XM_017017876.2:c.1651C= XP_016873365.1:p.Arg551=
XM_017017877.2:c.1651C= XP_016873366.1:p.Arg551=
XM_017017878.2:c.1651C= XP_016873367.1:p.Arg551=
XM_017017879.2:c.1651C= XP_016873368.1:p.Arg551=
XM_024448570.1:c.925C= XP_024304338.1:p.Arg309=
NM_017635.5:c.2167C= MANE Select NP_060105.3:p.Arg723=
NM_001300908.2:c.1447C= NP_001287837.1:p.Arg483=
NM_001369426.1:c.2167C= NP_001356355.1:p.Arg723=
NM_001369428.1:c.1651C= NP_001356357.1:p.Arg551=
NM_001369429.1:c.1651C= NP_001356358.1:p.Arg551=
NM_001369430.1:c.1651C= NP_001356359.1:p.Arg551=
NM_001369431.1:c.1651C= NP_001356360.1:p.Arg551=
NM_001369432.1:c.1651C= NP_001356361.1:p.Arg551=
NM_001369433.1:c.1651C= NP_001356362.1:p.Arg551=