Canonical Allele Identifier: CA475818851

Gene: CLPB

Linked Data

• MyVariant Identifiers: chr11:g.72114045T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72403001T>A , CM000673.2:g.72403001T>A	GRCh38
NC_000011.9:g.72114045T>A , CM000673.1:g.72114045T>A	GRCh37
NC_000011.8:g.71791693T>A	NCBI36
NG_042130.1:g.36684A>T
NG_042130.2:g.36684A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000535990.6:c.*107A>T	ENSP00000443822.2:n.*107A>T
ENST00000695924.1:n.578A>T
ENST00000695925.1:n.578A>T
ENST00000695926.1:n.578A>T
ENST00000294053.9:c.507A>T MANE Plus Clinical	ENSP00000294053.3:p.Thr169=
ENST00000535477.6:c.382A>T	ENSP00000440423.2:p.Ser128Cys
ENST00000538039.6:c.507A>T MANE Select	ENSP00000441518.1:p.Thr169=
ENST00000543042.6:c.507A>T	ENSP00000439746.2:p.Thr169=
ENST00000642288.1:c.-7A>T	ENSP00000495167.1:n.-7A>T
ENST00000646117.1:c.507A>T	ENSP00000495421.1:p.Thr169=
ENST00000294053.7:c.507A>T	ENSP00000294053.3:p.Thr169=
ENST00000340729.9:c.456-22617A>T	ENSP00000340385.5:n.456-22617A>T
ENST00000437826.6:c.372A>T	ENSP00000407296.2:p.Thr124=
ENST00000445069.4:n.334A>T
ENST00000535477.5:c.507A>T	ENSP00000440423.1:p.Thr169=
ENST00000535990.5:c.522A>T	ENSP00000443822.1:p.Thr174=
ENST00000538039.5:c.507A>T	ENSP00000441518.1:p.Thr169=
ENST00000539148.3:c.69A>T	ENSP00000445327.1:p.Thr23=
ENST00000543042.5:c.-7A>T	ENSP00000439746.1:n.-7A>T
ENST00000544683.5:c.69A>T	ENSP00000442651.1:p.Thr23=
NM_001258392.1:c.507A>T	NP_001245321.1:p.Thr169=
NM_001258392.2:c.507A>T	NP_001245321.1:p.Thr169=
NM_001258393.1:c.456-22617A>T	NP_001245322.1:n.456-22617A>T
NM_001258393.2:c.456-22617A>T	NP_001245322.1:n.456-22617A>T
NM_001258394.1:c.372A>T	NP_001245323.1:p.Thr124=
NM_001258394.2:c.372A>T	NP_001245323.1:p.Thr124=
NM_030813.4:c.507A>T	NP_110440.1:p.Thr169=
NM_030813.5:c.507A>T	NP_110440.1:p.Thr169=
XM_005274320.1:c.456-22617A>T	XP_005274377.1:n.456-22617A>T
XM_011545288.1:c.507A>T	XP_011543590.1:p.Thr169=
XM_011545289.1:c.507A>T	XP_011543591.1:p.Thr169=
XM_011545289.2:c.507A>T	XP_011543591.1:p.Thr169=
NM_001258392.3:c.507A>T MANE Select	NP_001245321.1:p.Thr169=
NM_001258393.3:c.456-22617A>T	NP_001245322.1:n.456-22617A>T
NM_030813.6:c.507A>T MANE Plus Clinical	NP_110440.1:p.Thr169=
NM_001258394.3:c.372A>T	NP_001245323.1:p.Thr124=