Canonical Allele Identifier: CA381725434

Gene: CLPB

Linked Data

• MyVariant Identifiers: chr11:g.72005094T>G (hg19) ; chr11:g.72294050T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72294050T>G , CM000673.2:g.72294050T>G	GRCh38
NC_000011.9:g.72005094T>G , CM000673.1:g.72005094T>G	GRCh37
NC_000011.8:g.71682742T>G	NCBI36
NG_042130.1:g.145635A>C
NG_042130.2:g.145635A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000535990.6:c.*1447A>C	ENSP00000443822.2:n.*1447A>C
ENST00000695924.1:n.2626A>C
ENST00000695925.1:n.3338A>C
ENST00000294053.9:c.1847A>C MANE Plus Clinical	ENSP00000294053.3:p.His616Pro
ENST00000535477.6:c.*1182A>C	ENSP00000440423.2:n.*1182A>C
ENST00000538039.6:c.1757A>C MANE Select	ENSP00000441518.1:p.His586Pro
ENST00000543042.6:c.1802A>C	ENSP00000439746.2:p.His601Pro
ENST00000642187.1:c.1265A>C	ENSP00000494594.1:n.1265A>C
ENST00000645105.1:n.1175A>C
ENST00000646359.1:n.935A>C
ENST00000294053.7:c.1847A>C	ENSP00000294053.3:p.His616Pro
ENST00000340729.9:c.1670A>C	ENSP00000340385.5:p.His557Pro
ENST00000437826.6:c.1712A>C	ENSP00000407296.2:p.His571Pro
ENST00000535477.5:c.*177A>C	ENSP00000440423.1:n.*177A>C
ENST00000535990.5:c.1862A>C	ENSP00000443822.1:p.His621Pro
ENST00000538021.5:c.774A>C	ENSP00000445180.2:n.774A>C
ENST00000538039.5:c.1757A>C	ENSP00000441518.1:p.His586Pro
ENST00000543042.5:c.1244A>C	ENSP00000439746.1:p.His415Pro
NM_001258392.1:c.1757A>C	NP_001245321.1:p.His586Pro
NM_001258392.2:c.1757A>C	NP_001245321.1:p.His586Pro
NM_001258393.1:c.1670A>C	NP_001245322.1:p.His557Pro
NM_001258393.2:c.1670A>C	NP_001245322.1:p.His557Pro
NM_001258394.1:c.1712A>C	NP_001245323.1:p.His571Pro
NM_001258394.2:c.1712A>C	NP_001245323.1:p.His571Pro
NM_030813.4:c.1847A>C	NP_110440.1:p.His616Pro
NM_030813.5:c.1847A>C	NP_110440.1:p.His616Pro
XM_005274320.1:c.1760A>C	XP_005274377.1:p.His587Pro
XM_011545288.1:c.1802A>C	XP_011543590.1:p.His601Pro
NM_001258392.3:c.1757A>C MANE Select	NP_001245321.1:p.His586Pro
NM_001258393.3:c.1670A>C	NP_001245322.1:p.His557Pro
NM_030813.6:c.1847A>C MANE Plus Clinical	NP_110440.1:p.His616Pro
NM_001258394.3:c.1712A>C	NP_001245323.1:p.His571Pro