Canonical Allele Identifier: CA6171343

Gene: CLPB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72317232G>C , CM000673.2:g.72317232G>C	GRCh38
NC_000011.9:g.72028276G>C , CM000673.1:g.72028276G>C	GRCh37
NC_000011.8:g.71705924G>C	NCBI36
NG_042130.1:g.122453C>G
NG_042130.2:g.122453C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001258392.3:c.874-12C>G MANE Select	NP_001245321.1:n.874-12C>G
ENST00000538039.6:c.874-12C>G MANE Select	ENSP00000441518.1:n.874-12C>G
NM_030813.6:c.964-12C>G MANE Plus Clinical	NP_110440.1:n.964-12C>G
ENST00000294053.9:c.964-12C>G MANE Plus Clinical	ENSP00000294053.3:n.964-12C>G
NM_001258392.1:c.874-12C>G	NP_001245321.1:n.874-12C>G
NM_001258392.2:c.874-12C>G	NP_001245321.1:n.874-12C>G
NM_001258393.1:c.787-12C>G	NP_001245322.1:n.787-12C>G
NM_001258393.2:c.787-12C>G	NP_001245322.1:n.787-12C>G
NM_001258393.3:c.787-12C>G	NP_001245322.1:n.787-12C>G
NM_001258394.1:c.829-12C>G	NP_001245323.1:n.829-12C>G
NM_001258394.2:c.829-12C>G	NP_001245323.1:n.829-12C>G
NM_001258394.3:c.829-12C>G	NP_001245323.1:n.829-12C>G
NM_030813.4:c.964-12C>G	NP_110440.1:n.964-12C>G
NM_030813.5:c.964-12C>G	NP_110440.1:n.964-12C>G
ENST00000294053.7:c.964-12C>G	ENSP00000294053.3:n.964-12C>G
ENST00000340729.9:c.787-12C>G	ENSP00000340385.5:n.787-12C>G
ENST00000437826.6:c.829-12C>G	ENSP00000407296.2:n.829-12C>G
ENST00000535477.5:c.874-12C>G	ENSP00000440423.1:n.874-12C>G
ENST00000535477.6:c.*299-12C>G	ENSP00000440423.2:n.*299-12C>G
ENST00000535990.5:c.979-12C>G	ENSP00000443822.1:n.979-12C>G
ENST00000535990.6:c.*564-12C>G	ENSP00000443822.2:n.*564-12C>G
ENST00000538039.5:c.874-12C>G	ENSP00000441518.1:n.874-12C>G
ENST00000543042.5:c.361-12C>G	ENSP00000439746.1:n.361-12C>G
ENST00000543042.6:c.964-12C>G	ENSP00000439746.2:n.964-12C>G
ENST00000544382.5:n.297-12C>G
ENST00000544683.5:c.436-12C>G	ENSP00000442651.1:n.436-12C>G
ENST00000642187.1:c.274-12C>G	ENSP00000494594.1:n.274-12C>G
ENST00000642288.1:c.361-12C>G	ENSP00000495167.1:n.361-12C>G
ENST00000645105.1:n.292-12C>G
ENST00000645650.1:n.218-12C>G
ENST00000695924.1:n.945-12C>G
ENST00000695925.1:n.945-12C>G
ENST00000695926.1:n.945-12C>G
XM_005274320.1:c.877-12C>G	XP_005274377.1:n.877-12C>G
XM_011545288.1:c.964-12C>G	XP_011543590.1:n.964-12C>G
XM_011545289.1:c.964-12C>G	XP_011543591.1:n.964-12C>G
XM_011545289.2:c.964-12C>G	XP_011543591.1:n.964-12C>G