Canonical Allele Identifier: CA1980499971

Gene: KMT5B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68157829_68157832delinsATCC , CM000673.2:g.68157829_68157832delinsATCC	GRCh38
NC_000011.9:g.67925296_67925299delinsATCC , CM000673.1:g.67925296_67925299delinsATCC	GRCh37
NC_000011.8:g.67681872_67681875delinsATCC	NCBI36
NG_052873.1:g.60941_60944delinsGGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453170.6:c.2301_2304delinsGGAT	ENSP00000406377.2:p.Glu767=
ENST00000524672.3:n.2866_2869delinsGGAT
ENST00000700520.1:c.*2138_*2141delinsGGAT	ENSP00000515027.1:n.*2138_*2141delinsGGAT
ENST00000700521.1:c.*2181_*2184delinsGGAT	ENSP00000515028.1:n.*2181_*2184delinsGGAT
ENST00000700522.1:c.*2181_*2184delinsGGAT	ENSP00000515029.1:n.*2181_*2184delinsGGAT
ENST00000700523.1:c.1998_2001delinsGGAT	ENSP00000515030.1:p.Glu666=
ENST00000700524.1:c.*1722_*1725delinsGGAT	ENSP00000515031.1:n.*1722_*1725delinsGGAT
ENST00000304363.9:c.2514_2517delinsGGAT MANE Select	ENSP00000305899.4:p.Glu838=
ENST00000304363.8:c.2514_2517delinsGGAT	ENSP00000305899.4:p.Glu838=
ENST00000441488.6:c.*1722_*1725delinsGGAT	ENSP00000411146.2:n.*1722_*1725delinsGGAT
ENST00000615954.4:c.2514_2517delinsGGAT	ENSP00000484858.1:p.Glu838=
NM_001300907.1:c.1998_2001delinsGGAT	NP_001287836.1:p.Glu666=
NM_001300908.1:c.1794_1797delinsGGAT	NP_001287837.1:p.Glu598=
NM_017635.4:c.2514_2517delinsGGAT	NP_060105.3:p.Glu838=
XM_005274035.2:c.2514_2517delinsGGAT	XP_005274092.2:p.Glu838=
XM_005274036.2:c.2445_2448delinsGGAT	XP_005274093.2:p.Glu815=
XM_005274037.1:c.1998_2001delinsGGAT	XP_005274094.1:p.Glu666=
XM_006718581.1:c.2445_2448delinsGGAT	XP_006718644.1:p.Glu815=
XM_011545091.1:c.2514_2517delinsGGAT	XP_011543393.1:p.Glu838=
XM_011545092.1:c.2301_2304delinsGGAT	XP_011543394.1:p.Glu767=
XM_011545093.1:c.1272_1275delinsGGAT	XP_011543395.1:p.Glu424=
XM_005274035.4:c.2514_2517delinsGGAT	XP_005274092.2:p.Glu838=
XM_005274036.4:c.2445_2448delinsGGAT	XP_005274093.2:p.Glu815=
XM_006718581.2:c.2445_2448delinsGGAT	XP_006718644.1:p.Glu815=
XM_011545092.3:c.2301_2304delinsGGAT	XP_011543394.1:p.Glu767=
XM_017017876.2:c.1998_2001delinsGGAT	XP_016873365.1:p.Glu666=
XM_017017877.2:c.1998_2001delinsGGAT	XP_016873366.1:p.Glu666=
XM_017017878.2:c.1998_2001delinsGGAT	XP_016873367.1:p.Glu666=
XM_017017879.2:c.1998_2001delinsGGAT	XP_016873368.1:p.Glu666=
XM_024448570.1:c.1272_1275delinsGGAT	XP_024304338.1:p.Glu424=
NM_017635.5:c.2514_2517delinsGGAT MANE Select	NP_060105.3:p.Glu838=
NM_001300908.2:c.1794_1797delinsGGAT	NP_001287837.1:p.Glu598=
NM_001369426.1:c.2514_2517delinsGGAT	NP_001356355.1:p.Glu838=
NM_001369428.1:c.1998_2001delinsGGAT	NP_001356357.1:p.Glu666=
NM_001369429.1:c.1998_2001delinsGGAT	NP_001356358.1:p.Glu666=
NM_001369430.1:c.1998_2001delinsGGAT	NP_001356359.1:p.Glu666=
NM_001369431.1:c.1998_2001delinsGGAT	NP_001356360.1:p.Glu666=
NM_001369432.1:c.1998_2001delinsGGAT	NP_001356361.1:p.Glu666=
NM_001369433.1:c.1998_2001delinsGGAT	NP_001356362.1:p.Glu666=