Canonical Allele Identifier: CA1980500600
Gene: KMT5B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68158154T= , CM000673.2:g.68158154T= GRCh38
NC_000011.9:g.67925621T= , CM000673.1:g.67925621T= GRCh37
NC_000011.8:g.67682197T= NCBI36
NG_052873.1:g.60619A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453170.6:c.1979A= ENSP00000406377.2:p.Asn660=
ENST00000524672.3:n.2544A=
ENST00000700520.1:c.*1816A= ENSP00000515027.1:n.*1816A=
ENST00000700521.1:c.*1859A= ENSP00000515028.1:n.*1859A=
ENST00000700522.1:c.*1859A= ENSP00000515029.1:n.*1859A=
ENST00000700523.1:c.1676A= ENSP00000515030.1:p.Asn559=
ENST00000700524.1:c.*1400A= ENSP00000515031.1:n.*1400A=
ENST00000304363.9:c.2192A= MANE Select ENSP00000305899.4:p.Asn731=
ENST00000304363.8:c.2192A= ENSP00000305899.4:p.Asn731=
ENST00000441488.6:c.*1400A= ENSP00000411146.2:n.*1400A=
ENST00000615954.4:c.2192A= ENSP00000484858.1:p.Asn731=
NM_001300907.1:c.1676A= NP_001287836.1:p.Asn559=
NM_001300908.1:c.1472A= NP_001287837.1:p.Asn491=
NM_017635.4:c.2192A= NP_060105.3:p.Asn731=
XM_005274035.2:c.2192A= XP_005274092.2:p.Asn731=
XM_005274036.2:c.2123A= XP_005274093.2:p.Asn708=
XM_005274037.1:c.1676A= XP_005274094.1:p.Asn559=
XM_006718581.1:c.2123A= XP_006718644.1:p.Asn708=
XM_011545091.1:c.2192A= XP_011543393.1:p.Asn731=
XM_011545092.1:c.1979A= XP_011543394.1:p.Asn660=
XM_011545093.1:c.950A= XP_011543395.1:p.Asn317=
XM_005274035.4:c.2192A= XP_005274092.2:p.Asn731=
XM_005274036.4:c.2123A= XP_005274093.2:p.Asn708=
XM_006718581.2:c.2123A= XP_006718644.1:p.Asn708=
XM_011545092.3:c.1979A= XP_011543394.1:p.Asn660=
XM_017017876.2:c.1676A= XP_016873365.1:p.Asn559=
XM_017017877.2:c.1676A= XP_016873366.1:p.Asn559=
XM_017017878.2:c.1676A= XP_016873367.1:p.Asn559=
XM_017017879.2:c.1676A= XP_016873368.1:p.Asn559=
XM_024448570.1:c.950A= XP_024304338.1:p.Asn317=
NM_017635.5:c.2192A= MANE Select NP_060105.3:p.Asn731=
NM_001300908.2:c.1472A= NP_001287837.1:p.Asn491=
NM_001369426.1:c.2192A= NP_001356355.1:p.Asn731=
NM_001369428.1:c.1676A= NP_001356357.1:p.Asn559=
NM_001369429.1:c.1676A= NP_001356358.1:p.Asn559=
NM_001369430.1:c.1676A= NP_001356359.1:p.Asn559=
NM_001369431.1:c.1676A= NP_001356360.1:p.Asn559=
NM_001369432.1:c.1676A= NP_001356361.1:p.Asn559=
NM_001369433.1:c.1676A= NP_001356362.1:p.Asn559=