Canonical Allele Identifier: CA475607702

Gene: CLPB

Linked Data

• gnomAD v4: 11-72302223-G-T
• MyVariant Identifiers: chr11:g.72013267G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72302223G>T , CM000673.2:g.72302223G>T	GRCh38
NC_000011.9:g.72013267G>T , CM000673.1:g.72013267G>T	GRCh37
NC_000011.8:g.71690915G>T	NCBI36
NG_042130.1:g.137462C>A
NG_042130.2:g.137462C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000535990.6:c.*857+81C>A	ENSP00000443822.2:n.*857+81C>A
ENST00000695924.1:n.1238+81C>A
ENST00000695925.1:n.1319C>A
ENST00000294053.9:c.1257+81C>A MANE Plus Clinical	ENSP00000294053.3:n.1257+81C>A
ENST00000535477.6:c.*592+81C>A	ENSP00000440423.2:n.*592+81C>A
ENST00000538039.6:c.1167+81C>A MANE Select	ENSP00000441518.1:n.1167+81C>A
ENST00000543042.6:c.1213-259C>A	ENSP00000439746.2:n.1213-259C>A
ENST00000642187.1:c.675+81C>A	ENSP00000494594.1:n.675+81C>A
ENST00000642288.1:c.654+81C>A	ENSP00000495167.1:n.654+81C>A
ENST00000645105.1:n.585+81C>A
ENST00000646359.1:n.345+81C>A
ENST00000294053.7:c.1257+81C>A	ENSP00000294053.3:n.1257+81C>A
ENST00000340729.9:c.1080+81C>A	ENSP00000340385.5:n.1080+81C>A
ENST00000437826.6:c.1122+81C>A	ENSP00000407296.2:n.1122+81C>A
ENST00000535477.5:c.1167+81C>A	ENSP00000440423.1:n.1167+81C>A
ENST00000535990.5:c.1272+81C>A	ENSP00000443822.1:n.1272+81C>A
ENST00000538021.5:c.184+81C>A	ENSP00000445180.2:n.184+81C>A
ENST00000538039.5:c.1167+81C>A	ENSP00000441518.1:n.1167+81C>A
ENST00000543042.5:c.654+81C>A	ENSP00000439746.1:n.654+81C>A
ENST00000544382.5:n.590+81C>A
NM_001258392.1:c.1167+81C>A	NP_001245321.1:n.1167+81C>A
NM_001258392.2:c.1167+81C>A	NP_001245321.1:n.1167+81C>A
NM_001258393.1:c.1080+81C>A	NP_001245322.1:n.1080+81C>A
NM_001258393.2:c.1080+81C>A	NP_001245322.1:n.1080+81C>A
NM_001258394.1:c.1122+81C>A	NP_001245323.1:n.1122+81C>A
NM_001258394.2:c.1122+81C>A	NP_001245323.1:n.1122+81C>A
NM_030813.4:c.1257+81C>A	NP_110440.1:n.1257+81C>A
NM_030813.5:c.1257+81C>A	NP_110440.1:n.1257+81C>A
XM_005274320.1:c.1170+81C>A	XP_005274377.1:n.1170+81C>A
XM_011545288.1:c.1213-259C>A	XP_011543590.1:n.1213-259C>A
XR_950282.1:n.1812G>T
XR_950283.1:n.1728-389G>T
NM_001258392.3:c.1167+81C>A MANE Select	NP_001245321.1:n.1167+81C>A
NM_001258393.3:c.1080+81C>A	NP_001245322.1:n.1080+81C>A
NM_030813.6:c.1257+81C>A MANE Plus Clinical	NP_110440.1:n.1257+81C>A
NM_001258394.3:c.1122+81C>A	NP_001245323.1:n.1122+81C>A