Canonical Allele Identifier: CA475607706

Gene: CLPB

Linked Data

• MyVariant Identifiers: chr11:g.72013269G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72302225G>A , CM000673.2:g.72302225G>A	GRCh38
NC_000011.9:g.72013269G>A , CM000673.1:g.72013269G>A	GRCh37
NC_000011.8:g.71690917G>A	NCBI36
NG_042130.1:g.137460C>T
NG_042130.2:g.137460C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000535990.6:c.*857+79C>T	ENSP00000443822.2:n.*857+79C>T
ENST00000695924.1:n.1238+79C>T
ENST00000695925.1:n.1317C>T
ENST00000294053.9:c.1257+79C>T MANE Plus Clinical	ENSP00000294053.3:n.1257+79C>T
ENST00000535477.6:c.*592+79C>T	ENSP00000440423.2:n.*592+79C>T
ENST00000538039.6:c.1167+79C>T MANE Select	ENSP00000441518.1:n.1167+79C>T
ENST00000543042.6:c.1213-261C>T	ENSP00000439746.2:n.1213-261C>T
ENST00000642187.1:c.675+79C>T	ENSP00000494594.1:n.675+79C>T
ENST00000642288.1:c.654+79C>T	ENSP00000495167.1:n.654+79C>T
ENST00000645105.1:n.585+79C>T
ENST00000646359.1:n.345+79C>T
ENST00000294053.7:c.1257+79C>T	ENSP00000294053.3:n.1257+79C>T
ENST00000340729.9:c.1080+79C>T	ENSP00000340385.5:n.1080+79C>T
ENST00000437826.6:c.1122+79C>T	ENSP00000407296.2:n.1122+79C>T
ENST00000535477.5:c.1167+79C>T	ENSP00000440423.1:n.1167+79C>T
ENST00000535990.5:c.1272+79C>T	ENSP00000443822.1:n.1272+79C>T
ENST00000538021.5:c.184+79C>T	ENSP00000445180.2:n.184+79C>T
ENST00000538039.5:c.1167+79C>T	ENSP00000441518.1:n.1167+79C>T
ENST00000543042.5:c.654+79C>T	ENSP00000439746.1:n.654+79C>T
ENST00000544382.5:n.590+79C>T
NM_001258392.1:c.1167+79C>T	NP_001245321.1:n.1167+79C>T
NM_001258392.2:c.1167+79C>T	NP_001245321.1:n.1167+79C>T
NM_001258393.1:c.1080+79C>T	NP_001245322.1:n.1080+79C>T
NM_001258393.2:c.1080+79C>T	NP_001245322.1:n.1080+79C>T
NM_001258394.1:c.1122+79C>T	NP_001245323.1:n.1122+79C>T
NM_001258394.2:c.1122+79C>T	NP_001245323.1:n.1122+79C>T
NM_030813.4:c.1257+79C>T	NP_110440.1:n.1257+79C>T
NM_030813.5:c.1257+79C>T	NP_110440.1:n.1257+79C>T
XM_005274320.1:c.1170+79C>T	XP_005274377.1:n.1170+79C>T
XM_011545288.1:c.1213-261C>T	XP_011543590.1:n.1213-261C>T
XR_950282.1:n.1814G>A
XR_950283.1:n.1728-387G>A
NM_001258392.3:c.1167+79C>T MANE Select	NP_001245321.1:n.1167+79C>T
NM_001258393.3:c.1080+79C>T	NP_001245322.1:n.1080+79C>T
NM_030813.6:c.1257+79C>T MANE Plus Clinical	NP_110440.1:n.1257+79C>T
NM_001258394.3:c.1122+79C>T	NP_001245323.1:n.1122+79C>T