Canonical Allele Identifier: CA381964613

Gene: CLPB

Linked Data

• MyVariant Identifiers: chr11:g.72114050A>T (hg19) ; chr11:g.72403006A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72403006A>T , CM000673.2:g.72403006A>T	GRCh38
NC_000011.9:g.72114050A>T , CM000673.1:g.72114050A>T	GRCh37
NC_000011.8:g.71791698A>T	NCBI36
NG_042130.1:g.36679T>A
NG_042130.2:g.36679T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000535990.6:c.*102T>A	ENSP00000443822.2:n.*102T>A
ENST00000695924.1:n.573T>A
ENST00000695925.1:n.573T>A
ENST00000695926.1:n.573T>A
ENST00000294053.9:c.502T>A MANE Plus Clinical	ENSP00000294053.3:p.Trp168Arg
ENST00000535477.6:c.377T>A	ENSP00000440423.2:p.Leu126Gln
ENST00000538039.6:c.502T>A MANE Select	ENSP00000441518.1:p.Trp168Arg
ENST00000543042.6:c.502T>A	ENSP00000439746.2:p.Trp168Arg
ENST00000642288.1:c.-12T>A	ENSP00000495167.1:n.-12T>A
ENST00000646117.1:c.502T>A	ENSP00000495421.1:p.Trp168Arg
ENST00000294053.7:c.502T>A	ENSP00000294053.3:p.Trp168Arg
ENST00000340729.9:c.456-22622T>A	ENSP00000340385.5:n.456-22622T>A
ENST00000437826.6:c.367T>A	ENSP00000407296.2:p.Trp123Arg
ENST00000445069.4:n.329T>A
ENST00000535477.5:c.502T>A	ENSP00000440423.1:p.Trp168Arg
ENST00000535990.5:c.517T>A	ENSP00000443822.1:p.Trp173Arg
ENST00000538039.5:c.502T>A	ENSP00000441518.1:p.Trp168Arg
ENST00000539148.3:c.64T>A	ENSP00000445327.1:p.Trp22Arg
ENST00000543042.5:c.-12T>A	ENSP00000439746.1:n.-12T>A
ENST00000544683.5:c.64T>A	ENSP00000442651.1:p.Trp22Arg
NM_001258392.1:c.502T>A	NP_001245321.1:p.Trp168Arg
NM_001258392.2:c.502T>A	NP_001245321.1:p.Trp168Arg
NM_001258393.1:c.456-22622T>A	NP_001245322.1:n.456-22622T>A
NM_001258393.2:c.456-22622T>A	NP_001245322.1:n.456-22622T>A
NM_001258394.1:c.367T>A	NP_001245323.1:p.Trp123Arg
NM_001258394.2:c.367T>A	NP_001245323.1:p.Trp123Arg
NM_030813.4:c.502T>A	NP_110440.1:p.Trp168Arg
NM_030813.5:c.502T>A	NP_110440.1:p.Trp168Arg
XM_005274320.1:c.456-22622T>A	XP_005274377.1:n.456-22622T>A
XM_011545288.1:c.502T>A	XP_011543590.1:p.Trp168Arg
XM_011545289.1:c.502T>A	XP_011543591.1:p.Trp168Arg
XM_011545289.2:c.502T>A	XP_011543591.1:p.Trp168Arg
NM_001258392.3:c.502T>A MANE Select	NP_001245321.1:p.Trp168Arg
NM_001258393.3:c.456-22622T>A	NP_001245322.1:n.456-22622T>A
NM_030813.6:c.502T>A MANE Plus Clinical	NP_110440.1:p.Trp168Arg
NM_001258394.3:c.367T>A	NP_001245323.1:p.Trp123Arg