Canonical Allele Identifier: CA475514452
Gene: KMT5B HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67925227A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68157760A>T , CM000673.2:g.68157760A>T GRCh38
NC_000011.9:g.67925227A>T , CM000673.1:g.67925227A>T GRCh37
NC_000011.8:g.67681803A>T NCBI36
NG_052873.1:g.61013T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000453170.6:c.2373T>A ENSP00000406377.2:p.Val791=
ENST00000524672.3:n.2938T>A
ENST00000700520.1:c.*2210T>A ENSP00000515027.1:n.*2210T>A
ENST00000700521.1:c.*2253T>A ENSP00000515028.1:n.*2253T>A
ENST00000700522.1:c.*2253T>A ENSP00000515029.1:n.*2253T>A
ENST00000700523.1:c.2070T>A ENSP00000515030.1:p.Val690=
ENST00000700524.1:c.*1794T>A ENSP00000515031.1:n.*1794T>A
ENST00000304363.9:c.2586T>A MANE Select ENSP00000305899.4:p.Val862=
ENST00000304363.8:c.2586T>A ENSP00000305899.4:p.Val862=
ENST00000441488.6:c.*1794T>A ENSP00000411146.2:n.*1794T>A
ENST00000615954.4:c.2586T>A ENSP00000484858.1:p.Val862=
NM_001300907.1:c.2070T>A NP_001287836.1:p.Val690=
NM_001300908.1:c.1866T>A NP_001287837.1:p.Val622=
NM_017635.4:c.2586T>A NP_060105.3:p.Val862=
XM_005274035.2:c.2586T>A XP_005274092.2:p.Val862=
XM_005274036.2:c.2517T>A XP_005274093.2:p.Val839=
XM_005274037.1:c.2070T>A XP_005274094.1:p.Val690=
XM_006718581.1:c.2517T>A XP_006718644.1:p.Val839=
XM_011545091.1:c.2586T>A XP_011543393.1:p.Val862=
XM_011545092.1:c.2373T>A XP_011543394.1:p.Val791=
XM_011545093.1:c.1344T>A XP_011543395.1:p.Val448=
XM_005274035.4:c.2586T>A XP_005274092.2:p.Val862=
XM_005274036.4:c.2517T>A XP_005274093.2:p.Val839=
XM_006718581.2:c.2517T>A XP_006718644.1:p.Val839=
XM_011545092.3:c.2373T>A XP_011543394.1:p.Val791=
XM_017017876.2:c.2070T>A XP_016873365.1:p.Val690=
XM_017017877.2:c.2070T>A XP_016873366.1:p.Val690=
XM_017017878.2:c.2070T>A XP_016873367.1:p.Val690=
XM_017017879.2:c.2070T>A XP_016873368.1:p.Val690=
XM_024448570.1:c.1344T>A XP_024304338.1:p.Val448=
NM_017635.5:c.2586T>A MANE Select NP_060105.3:p.Val862=
NM_001300908.2:c.1866T>A NP_001287837.1:p.Val622=
NM_001369426.1:c.2586T>A NP_001356355.1:p.Val862=
NM_001369428.1:c.2070T>A NP_001356357.1:p.Val690=
NM_001369429.1:c.2070T>A NP_001356358.1:p.Val690=
NM_001369430.1:c.2070T>A NP_001356359.1:p.Val690=
NM_001369431.1:c.2070T>A NP_001356360.1:p.Val690=
NM_001369432.1:c.2070T>A NP_001356361.1:p.Val690=
NM_001369433.1:c.2070T>A NP_001356362.1:p.Val690=