Canonical Allele Identifier: CA600087838

Gene: CLPB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72329809C>A , CM000673.2:g.72329809C>A	GRCh38
NC_000011.9:g.72040853C>A , CM000673.1:g.72040853C>A	GRCh37
NC_000011.8:g.71718501C>A	NCBI36
NG_042130.1:g.109876G>T
NG_042130.2:g.109876G>T

Transcript Alleles

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