Canonical Allele Identifier: CA600179444

Gene: CLPB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72358860T>C , CM000673.2:g.72358860T>C	GRCh38
NC_000011.9:g.72069904T>C , CM000673.1:g.72069904T>C	GRCh37
NC_000011.8:g.71747552T>C	NCBI36
NG_042130.1:g.80825A>G
NG_042130.2:g.80825A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001258392.3:c.775+20A>G MANE Select	NP_001245321.1:n.775+20A>G
ENST00000538039.6:c.775+20A>G MANE Select	ENSP00000441518.1:n.775+20A>G
NM_030813.6:c.865+20A>G MANE Plus Clinical	NP_110440.1:n.865+20A>G
ENST00000294053.9:c.865+20A>G MANE Plus Clinical	ENSP00000294053.3:n.865+20A>G
NM_001258392.1:c.775+20A>G	NP_001245321.1:n.775+20A>G
NM_001258392.2:c.775+20A>G	NP_001245321.1:n.775+20A>G
NM_001258393.1:c.688+20A>G	NP_001245322.1:n.688+20A>G
NM_001258393.2:c.688+20A>G	NP_001245322.1:n.688+20A>G
NM_001258393.3:c.688+20A>G	NP_001245322.1:n.688+20A>G
NM_001258394.1:c.730+20A>G	NP_001245323.1:n.730+20A>G
NM_001258394.2:c.730+20A>G	NP_001245323.1:n.730+20A>G
NM_001258394.3:c.730+20A>G	NP_001245323.1:n.730+20A>G
NM_030813.4:c.865+20A>G	NP_110440.1:n.865+20A>G
NM_030813.5:c.865+20A>G	NP_110440.1:n.865+20A>G
ENST00000294053.7:c.865+20A>G	ENSP00000294053.3:n.865+20A>G
ENST00000340729.9:c.688+20A>G	ENSP00000340385.5:n.688+20A>G
ENST00000437826.6:c.730+20A>G	ENSP00000407296.2:n.730+20A>G
ENST00000445069.4:n.692+20A>G
ENST00000535477.5:c.775+20A>G	ENSP00000440423.1:n.775+20A>G
ENST00000535477.6:c.*200+20A>G	ENSP00000440423.2:n.*200+20A>G
ENST00000535990.5:c.880+20A>G	ENSP00000443822.1:n.880+20A>G
ENST00000535990.6:c.*465+20A>G	ENSP00000443822.2:n.*465+20A>G
ENST00000536297.1:c.241+20A>G
ENST00000538039.5:c.775+20A>G	ENSP00000441518.1:n.775+20A>G
ENST00000539148.3:c.427+20A>G	ENSP00000445327.1:n.427+20A>G
ENST00000543042.5:c.262+20A>G	ENSP00000439746.1:n.262+20A>G
ENST00000543042.6:c.865+20A>G	ENSP00000439746.2:n.865+20A>G
ENST00000544382.5:n.198+20A>G
ENST00000544683.5:c.337+20A>G	ENSP00000442651.1:n.337+20A>G
ENST00000642187.1:c.175+20A>G	ENSP00000494594.1:n.175+20A>G
ENST00000642288.1:c.262+20A>G	ENSP00000495167.1:n.262+20A>G
ENST00000646117.1:c.865+20A>G	ENSP00000495421.1:n.865+20A>G
ENST00000695924.1:n.846+20A>G
ENST00000695925.1:n.846+20A>G
ENST00000695926.1:n.846+20A>G
XM_005274320.1:c.778+20A>G	XP_005274377.1:n.778+20A>G
XM_011545288.1:c.865+20A>G	XP_011543590.1:n.865+20A>G
XM_011545289.1:c.865+20A>G	XP_011543591.1:n.865+20A>G
XM_011545289.2:c.865+20A>G	XP_011543591.1:n.865+20A>G