Canonical Allele Identifier: CA6171381

Gene: CLPB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72329814G>C , CM000673.2:g.72329814G>C	GRCh38
NC_000011.9:g.72040858G>C , CM000673.1:g.72040858G>C	GRCh37
NC_000011.8:g.71718506G>C	NCBI36
NG_042130.1:g.109871C>G
NG_042130.2:g.109871C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001258392.3:c.776-10C>G MANE Select	NP_001245321.1:n.776-10C>G
ENST00000538039.6:c.776-10C>G MANE Select	ENSP00000441518.1:n.776-10C>G
NM_030813.6:c.866-10C>G MANE Plus Clinical	NP_110440.1:n.866-10C>G
ENST00000294053.9:c.866-10C>G MANE Plus Clinical	ENSP00000294053.3:n.866-10C>G
NM_001258392.1:c.776-10C>G	NP_001245321.1:n.776-10C>G
NM_001258392.2:c.776-10C>G	NP_001245321.1:n.776-10C>G
NM_001258393.1:c.689-10C>G	NP_001245322.1:n.689-10C>G
NM_001258393.2:c.689-10C>G	NP_001245322.1:n.689-10C>G
NM_001258393.3:c.689-10C>G	NP_001245322.1:n.689-10C>G
NM_001258394.1:c.731-10C>G	NP_001245323.1:n.731-10C>G
NM_001258394.2:c.731-10C>G	NP_001245323.1:n.731-10C>G
NM_001258394.3:c.731-10C>G	NP_001245323.1:n.731-10C>G
NM_030813.4:c.866-10C>G	NP_110440.1:n.866-10C>G
NM_030813.5:c.866-10C>G	NP_110440.1:n.866-10C>G
ENST00000294053.7:c.866-10C>G	ENSP00000294053.3:n.866-10C>G
ENST00000340729.9:c.689-10C>G	ENSP00000340385.5:n.689-10C>G
ENST00000437826.6:c.731-10C>G	ENSP00000407296.2:n.731-10C>G
ENST00000535477.5:c.776-10C>G	ENSP00000440423.1:n.776-10C>G
ENST00000535477.6:c.*201-10C>G	ENSP00000440423.2:n.*201-10C>G
ENST00000535990.5:c.881-10C>G	ENSP00000443822.1:n.881-10C>G
ENST00000535990.6:c.*466-10C>G	ENSP00000443822.2:n.*466-10C>G
ENST00000538039.5:c.776-10C>G	ENSP00000441518.1:n.776-10C>G
ENST00000539148.3:c.428-10C>G	ENSP00000445327.1:n.428-10C>G
ENST00000543042.5:c.263-10C>G	ENSP00000439746.1:n.263-10C>G
ENST00000543042.6:c.866-10C>G	ENSP00000439746.2:n.866-10C>G
ENST00000544382.5:n.199-10C>G
ENST00000544683.5:c.338-10C>G	ENSP00000442651.1:n.338-10C>G
ENST00000642187.1:c.176-10C>G	ENSP00000494594.1:n.176-10C>G
ENST00000642288.1:c.263-10C>G	ENSP00000495167.1:n.263-10C>G
ENST00000645105.1:n.194-10C>G
ENST00000645650.1:n.120-10C>G
ENST00000695924.1:n.847-10C>G
ENST00000695925.1:n.847-10C>G
ENST00000695926.1:n.847-10C>G
XM_005274320.1:c.779-10C>G	XP_005274377.1:n.779-10C>G
XM_011545288.1:c.866-10C>G	XP_011543590.1:n.866-10C>G
XM_011545289.1:c.866-10C>G	XP_011543591.1:n.866-10C>G
XM_011545289.2:c.866-10C>G	XP_011543591.1:n.866-10C>G