Canonical Allele Identifier: CA224386158
Gene: CLPB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72294941_72294947dup , CM000673.2:g.72294941_72294947dup GRCh38
NC_000011.9:g.72005985_72005991dup , CM000673.1:g.72005985_72005991dup GRCh37
NC_000011.8:g.71683633_71683639dup NCBI36
NG_042130.1:g.144741_144747dup
NG_042130.2:g.144741_144747dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000535990.6:c.*1177-251_*1177-245dup ENSP00000443822.2:n.*1177-251_*1177-245dup
ENST00000695924.1:n.2105_2111dup
ENST00000695925.1:n.2444_2450dup
ENST00000294053.9:c.1577-251_1577-245dup MANE Plus Clinical ENSP00000294053.3:n.1577-251_1577-245dup
ENST00000535477.6:c.*912-251_*912-245dup ENSP00000440423.2:n.*912-251_*912-245dup
ENST00000538039.6:c.1487-251_1487-245dup MANE Select ENSP00000441518.1:n.1487-251_1487-245dup
ENST00000543042.6:c.1532-251_1532-245dup ENSP00000439746.2:n.1532-251_1532-245dup
ENST00000642187.1:c.995-251_995-245dup ENSP00000494594.1:n.995-251_995-245dup
ENST00000642288.1:c.974-251_974-245dup ENSP00000495167.1:n.974-251_974-245dup
ENST00000645105.1:n.905-251_905-245dup
ENST00000646359.1:n.665-251_665-245dup
ENST00000294053.7:c.1577-251_1577-245dup ENSP00000294053.3:n.1577-251_1577-245dup
ENST00000340729.9:c.1400-251_1400-245dup ENSP00000340385.5:n.1400-251_1400-245dup
ENST00000437826.6:c.1442-251_1442-245dup ENSP00000407296.2:n.1442-251_1442-245dup
ENST00000535477.5:c.1487-500_1487-494dup ENSP00000440423.1:n.1487-500_1487-494dup
ENST00000535990.5:c.1592-251_1592-245dup ENSP00000443822.1:n.1592-251_1592-245dup
ENST00000538021.5:c.504-251_504-245dup ENSP00000445180.2:n.504-251_504-245dup
ENST00000538039.5:c.1487-251_1487-245dup ENSP00000441518.1:n.1487-251_1487-245dup
ENST00000543042.5:c.974-251_974-245dup ENSP00000439746.1:n.974-251_974-245dup
ENST00000544382.5:n.910-251_910-245dup
NM_001258392.1:c.1487-251_1487-245dup NP_001245321.1:n.1487-251_1487-245dup
NM_001258392.2:c.1487-251_1487-245dup NP_001245321.1:n.1487-251_1487-245dup
NM_001258393.1:c.1400-251_1400-245dup NP_001245322.1:n.1400-251_1400-245dup
NM_001258393.2:c.1400-251_1400-245dup NP_001245322.1:n.1400-251_1400-245dup
NM_001258394.1:c.1442-251_1442-245dup NP_001245323.1:n.1442-251_1442-245dup
NM_001258394.2:c.1442-251_1442-245dup NP_001245323.1:n.1442-251_1442-245dup
NM_030813.4:c.1577-251_1577-245dup NP_110440.1:n.1577-251_1577-245dup
NM_030813.5:c.1577-251_1577-245dup NP_110440.1:n.1577-251_1577-245dup
XM_005274320.1:c.1490-251_1490-245dup XP_005274377.1:n.1490-251_1490-245dup
XM_011545288.1:c.1532-251_1532-245dup XP_011543590.1:n.1532-251_1532-245dup
NM_001258392.3:c.1487-251_1487-245dup MANE Select NP_001245321.1:n.1487-251_1487-245dup
NM_001258393.3:c.1400-251_1400-245dup NP_001245322.1:n.1400-251_1400-245dup
NM_030813.6:c.1577-251_1577-245dup MANE Plus Clinical NP_110440.1:n.1577-251_1577-245dup
NM_001258394.3:c.1442-251_1442-245dup NP_001245323.1:n.1442-251_1442-245dup