Canonical Allele Identifier: CA2580615744

Gene: KMT5B

Linked Data

• ClinVar Variation Id: 2573668
• ClinVar RCV Id: RCV003318004

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68158169_68158170delinsG , CM000673.2:g.68158169_68158170delinsG	GRCh38
NC_000011.9:g.67925636_67925637delinsG , CM000673.1:g.67925636_67925637delinsG	GRCh37
NC_000011.8:g.67682212_67682213delinsG	NCBI36
NG_052873.1:g.60603_60604delinsC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453170.6:c.1963_1964delinsC	ENSP00000406377.2:p.Ser655ProfsTer13
ENST00000524672.3:n.2528_2529delinsC
ENST00000700520.1:c.*1800_*1801delinsC	ENSP00000515027.1:n.*1800_*1801delinsC
ENST00000700521.1:c.*1843_*1844delinsC	ENSP00000515028.1:n.*1843_*1844delinsC
ENST00000700522.1:c.*1843_*1844delinsC	ENSP00000515029.1:n.*1843_*1844delinsC
ENST00000700523.1:c.1660_1661delinsC	ENSP00000515030.1:p.Ser554ProfsTer13
ENST00000700524.1:c.*1384_*1385delinsC	ENSP00000515031.1:n.*1384_*1385delinsC
ENST00000304363.9:c.2176_2177delinsC MANE Select	ENSP00000305899.4:p.Ser726ProfsTer13
ENST00000304363.8:c.2176_2177delinsC	ENSP00000305899.4:p.Ser726ProfsTer13
ENST00000441488.6:c.*1384_*1385delinsC	ENSP00000411146.2:n.*1384_*1385delinsC
ENST00000615954.4:c.2176_2177delinsC	ENSP00000484858.1:p.Ser726ProfsTer13
NM_001300907.1:c.1660_1661delinsC	NP_001287836.1:p.Ser554ProfsTer13
NM_001300908.1:c.1456_1457delinsC	NP_001287837.1:p.Ser486ProfsTer13
NM_017635.4:c.2176_2177delinsC	NP_060105.3:p.Ser726ProfsTer13
XM_005274035.2:c.2176_2177delinsC	XP_005274092.2:p.Ser726ProfsTer13
XM_005274036.2:c.2107_2108delinsC	XP_005274093.2:p.Ser703ProfsTer13
XM_005274037.1:c.1660_1661delinsC	XP_005274094.1:p.Ser554ProfsTer13
XM_006718581.1:c.2107_2108delinsC	XP_006718644.1:p.Ser703ProfsTer13
XM_011545091.1:c.2176_2177delinsC	XP_011543393.1:p.Ser726ProfsTer13
XM_011545092.1:c.1963_1964delinsC	XP_011543394.1:p.Ser655ProfsTer13
XM_011545093.1:c.934_935delinsC	XP_011543395.1:p.Ser312ProfsTer13
XM_005274035.4:c.2176_2177delinsC	XP_005274092.2:p.Ser726ProfsTer13
XM_005274036.4:c.2107_2108delinsC	XP_005274093.2:p.Ser703ProfsTer13
XM_006718581.2:c.2107_2108delinsC	XP_006718644.1:p.Ser703ProfsTer13
XM_011545092.3:c.1963_1964delinsC	XP_011543394.1:p.Ser655ProfsTer13
XM_017017876.2:c.1660_1661delinsC	XP_016873365.1:p.Ser554ProfsTer13
XM_017017877.2:c.1660_1661delinsC	XP_016873366.1:p.Ser554ProfsTer13
XM_017017878.2:c.1660_1661delinsC	XP_016873367.1:p.Ser554ProfsTer13
XM_017017879.2:c.1660_1661delinsC	XP_016873368.1:p.Ser554ProfsTer13
XM_024448570.1:c.934_935delinsC	XP_024304338.1:p.Ser312ProfsTer13
NM_017635.5:c.2176_2177delinsC MANE Select	NP_060105.3:p.Ser726ProfsTer13
NM_001300908.2:c.1456_1457delinsC	NP_001287837.1:p.Ser486ProfsTer13
NM_001369426.1:c.2176_2177delinsC	NP_001356355.1:p.Ser726ProfsTer13
NM_001369428.1:c.1660_1661delinsC	NP_001356357.1:p.Ser554ProfsTer13
NM_001369429.1:c.1660_1661delinsC	NP_001356358.1:p.Ser554ProfsTer13
NM_001369430.1:c.1660_1661delinsC	NP_001356359.1:p.Ser554ProfsTer13
NM_001369431.1:c.1660_1661delinsC	NP_001356360.1:p.Ser554ProfsTer13
NM_001369432.1:c.1660_1661delinsC	NP_001356361.1:p.Ser554ProfsTer13
NM_001369433.1:c.1660_1661delinsC	NP_001356362.1:p.Ser554ProfsTer13