Canonical Allele Identifier: CA6171297

Gene: CLPB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72308597C>T , CM000673.2:g.72308597C>T	GRCh38
NC_000011.9:g.72019641C>T , CM000673.1:g.72019641C>T	GRCh37
NC_000011.8:g.71697289C>T	NCBI36
NG_042130.1:g.131088G>A
NG_042130.2:g.131088G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000535990.6:c.*686G>A	ENSP00000443822.2:n.*686G>A
ENST00000695924.1:n.1067G>A
ENST00000695925.1:n.1067G>A
ENST00000294053.9:c.1086G>A MANE Plus Clinical	ENSP00000294053.3:p.Arg362=
ENST00000535477.6:c.*421G>A	ENSP00000440423.2:n.*421G>A
ENST00000538039.6:c.996G>A MANE Select	ENSP00000441518.1:p.Arg332=
ENST00000543042.6:c.1086G>A	ENSP00000439746.2:p.Arg362=
ENST00000642187.1:c.504G>A	ENSP00000494594.1:n.504G>A
ENST00000642288.1:c.483G>A	ENSP00000495167.1:p.Arg161=
ENST00000645105.1:n.414G>A
ENST00000645650.1:n.340G>A
ENST00000294053.7:c.1086G>A	ENSP00000294053.3:p.Arg362=
ENST00000340729.9:c.909G>A	ENSP00000340385.5:p.Arg303=
ENST00000437826.6:c.951G>A	ENSP00000407296.2:p.Arg317=
ENST00000535477.5:c.996G>A	ENSP00000440423.1:p.Arg332=
ENST00000535990.5:c.1101G>A	ENSP00000443822.1:p.Arg367=
ENST00000538039.5:c.996G>A	ENSP00000441518.1:p.Arg332=
ENST00000543042.5:c.483G>A	ENSP00000439746.1:p.Arg161=
ENST00000544382.5:n.419G>A
NM_001258392.1:c.996G>A	NP_001245321.1:p.Arg332=
NM_001258392.2:c.996G>A	NP_001245321.1:p.Arg332=
NM_001258393.1:c.909G>A	NP_001245322.1:p.Arg303=
NM_001258393.2:c.909G>A	NP_001245322.1:p.Arg303=
NM_001258394.1:c.951G>A	NP_001245323.1:p.Arg317=
NM_001258394.2:c.951G>A	NP_001245323.1:p.Arg317=
NM_030813.4:c.1086G>A	NP_110440.1:p.Arg362=
NM_030813.5:c.1086G>A	NP_110440.1:p.Arg362=
XM_005274320.1:c.999G>A	XP_005274377.1:p.Arg333=
XM_011545288.1:c.1086G>A	XP_011543590.1:p.Arg362=
NM_001258392.3:c.996G>A MANE Select	NP_001245321.1:p.Arg332=
NM_001258393.3:c.909G>A	NP_001245322.1:p.Arg303=
NM_030813.6:c.1086G>A MANE Plus Clinical	NP_110440.1:p.Arg362=
NM_001258394.3:c.951G>A	NP_001245323.1:p.Arg317=