Canonical Allele Identifier: CA475514887

Gene: KMT5B

Linked Data

• MyVariant Identifiers: chr11:g.67925726_67925727insA (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68158259_68158260insA , CM000673.2:g.68158259_68158260insA	GRCh38
NC_000011.9:g.67925726_67925727insA , CM000673.1:g.67925726_67925727insA	GRCh37
NC_000011.8:g.67682302_67682303insA	NCBI36
NG_052873.1:g.60513_60514insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453170.6:c.1873_1874insT	ENSP00000406377.2:p.Lys625IlefsTer9
ENST00000524672.3:n.2438_2439insT
ENST00000700520.1:c.*1710_*1711insT	ENSP00000515027.1:n.*1710_*1711insT
ENST00000700521.1:c.*1753_*1754insT	ENSP00000515028.1:n.*1753_*1754insT
ENST00000700522.1:c.*1753_*1754insT	ENSP00000515029.1:n.*1753_*1754insT
ENST00000700523.1:c.1570_1571insT	ENSP00000515030.1:p.Lys524IlefsTer9
ENST00000700524.1:c.*1294_*1295insT	ENSP00000515031.1:n.*1294_*1295insT
ENST00000304363.9:c.2086_2087insT MANE Select	ENSP00000305899.4:p.Lys696IlefsTer9
ENST00000304363.8:c.2086_2087insT	ENSP00000305899.4:p.Lys696IlefsTer9
ENST00000441488.6:c.*1294_*1295insT	ENSP00000411146.2:n.*1294_*1295insT
ENST00000615954.4:c.2086_2087insT	ENSP00000484858.1:p.Lys696IlefsTer9
NM_001300907.1:c.1570_1571insT	NP_001287836.1:p.Lys524IlefsTer9
NM_001300908.1:c.1366_1367insT	NP_001287837.1:p.Lys456IlefsTer9
NM_017635.4:c.2086_2087insT	NP_060105.3:p.Lys696IlefsTer9
XM_005274035.2:c.2086_2087insT	XP_005274092.2:p.Lys696IlefsTer9
XM_005274036.2:c.2017_2018insT	XP_005274093.2:p.Lys673IlefsTer9
XM_005274037.1:c.1570_1571insT	XP_005274094.1:p.Lys524IlefsTer9
XM_006718581.1:c.2017_2018insT	XP_006718644.1:p.Lys673IlefsTer9
XM_011545091.1:c.2086_2087insT	XP_011543393.1:p.Lys696IlefsTer9
XM_011545092.1:c.1873_1874insT	XP_011543394.1:p.Lys625IlefsTer9
XM_011545093.1:c.844_845insT	XP_011543395.1:p.Lys282IlefsTer9
XM_005274035.4:c.2086_2087insT	XP_005274092.2:p.Lys696IlefsTer9
XM_005274036.4:c.2017_2018insT	XP_005274093.2:p.Lys673IlefsTer9
XM_006718581.2:c.2017_2018insT	XP_006718644.1:p.Lys673IlefsTer9
XM_011545092.3:c.1873_1874insT	XP_011543394.1:p.Lys625IlefsTer9
XM_017017876.2:c.1570_1571insT	XP_016873365.1:p.Lys524IlefsTer9
XM_017017877.2:c.1570_1571insT	XP_016873366.1:p.Lys524IlefsTer9
XM_017017878.2:c.1570_1571insT	XP_016873367.1:p.Lys524IlefsTer9
XM_017017879.2:c.1570_1571insT	XP_016873368.1:p.Lys524IlefsTer9
XM_024448570.1:c.844_845insT	XP_024304338.1:p.Lys282IlefsTer9
NM_017635.5:c.2086_2087insT MANE Select	NP_060105.3:p.Lys696IlefsTer9
NM_001300908.2:c.1366_1367insT	NP_001287837.1:p.Lys456IlefsTer9
NM_001369426.1:c.2086_2087insT	NP_001356355.1:p.Lys696IlefsTer9
NM_001369428.1:c.1570_1571insT	NP_001356357.1:p.Lys524IlefsTer9
NM_001369429.1:c.1570_1571insT	NP_001356358.1:p.Lys524IlefsTer9
NM_001369430.1:c.1570_1571insT	NP_001356359.1:p.Lys524IlefsTer9
NM_001369431.1:c.1570_1571insT	NP_001356360.1:p.Lys524IlefsTer9
NM_001369432.1:c.1570_1571insT	NP_001356361.1:p.Lys524IlefsTer9
NM_001369433.1:c.1570_1571insT	NP_001356362.1:p.Lys524IlefsTer9