Canonical Allele Identifier: CA1088396475

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43523209_43523210insGGTCCTTGGAGGTACTATACAGTATCAAGTATAGTACCTCTAAAGACTG , CM000668.2:g.43523209_43523210insGGTCCTTGGAGGTACTATACAGTATCAAGTATAGTACCTCTAAAGACTG GRCh38
NC_000006.11:g.43490947_43490948insGGTCCTTGGAGGTACTATACAGTATCAAGTATAGTACCTCTAAAGACTG , CM000668.1:g.43490947_43490948insGGTCCTTGGAGGTACTATACAGTATCAAGTATAGTACCTCTAAAGACTG GRCh37
NC_000006.10:g.43598925_43598926insGGTCCTTGGAGGTACTATACAGTATCAAGTATAGTACCTCTAAAGACTG NCBI36
NG_028283.1:g.11171_11172insGGTCCTTGGAGGTACTATACAGTATCAAGTATAGTACCTCTAAAGACTG
NG_028283.3:g.18508_18509insGGTCCTTGGAGGTACTATACAGTATCAAGTATAGTACCTCTAAAGACTG
NG_051658.1:g.57866_57867insCAGTCTTTAGAGGTACTATACTTGATACTGTATAGTACCTCCAAGGACC

Transcript Alleles

HGVS Amino-acid Change
ENST00000265351.12:c.*658_*659insCAGTCTTTAGAGGTACTATACTTGATACTGTATAGTACCTCCAAGGACC (XPO5) MANE Select ENSP00000265351.7:n.*658_*659insCAGTCTTTAGAGGTACTATACTTGATACT...
ENST00000607635.2:c.922+2161_922+2162insGGTCCTTGGAGGTACTATACAGTATCAAGTATAGTACCTCTAAAGACTG (POLR1C) ENSP00000496683.1:n.922+2161_922+2162insGGTCCTTGGAGGTACTATACA...
ENST00000643341.1:c.922+2161_922+2162insGGTCCTTGGAGGTACTATACAGTATCAAGTATAGTACCTCTAAAGACTG (POLR1C) ENSP00000496018.1:n.922+2161_922+2162insGGTCCTTGGAGGTACTATACA...
ENST00000643799.1:c.*17+1892_*17+1893insGGTCCTTGGAGGTACTATACAGTATCAAGTATAGTACCTCTAAAGACTG (POLR1C) ENSP00000494529.1:n.*17+1892_*17+1893insGGTCCTTGGAGGTACTATACA...
ENST00000646433.1:c.922+2161_922+2162insGGTCCTTGGAGGTACTATACAGTATCAAGTATAGTACCTCTAAAGACTG (POLR1C) ENSP00000494368.1:n.922+2161_922+2162insGGTCCTTGGAGGTACTATACA...
ENST00000646700.1:c.922+2161_922+2162insGGTCCTTGGAGGTACTATACAGTATCAAGTATAGTACCTCTAAAGACTG (POLR1C) ENSP00000495521.1:n.922+2161_922+2162insGGTCCTTGGAGGTACTATACA...
ENST00000265351.11:c.*658_*659insCAGTCTTTAGAGGTACTATACTTGATACTGTATAGTACCTCCAAGGACC (XPO5) ENSP00000265351.7:n.*658_*659insCAGTCTTTAGAGGTACTATACTTGATACT...
ENST00000304004.7:c.922+2161_922+2162insGGTCCTTGGAGGTACTATACAGTATCAAGTATAGTACCTCTAAAGACTG (POLR1C) ENSP00000307212.3:n.922+2161_922+2162insGGTCCTTGGAGGTACTATACA...
ENST00000455854.2:n.2756_2757insCAGTCTTTAGAGGTACTATACTTGATACTGTATAGTACCTCCAAGGACC (XPO5)
NM_020750.2:c.*658_*659insCAGTCTTTAGAGGTACTATACTTGATACTGTATAGTACCTCCAAGGACC (XPO5) NP_065801.1:n.*658_*659insCAGTCTTTAGAGGTACTATACTTGATACTGTATAG...
XM_005249491.1:c.922+2161_922+2162insGGTCCTTGGAGGTACTATACAGTATCAAGTATAGTACCTCTAAAGACTG (POLR1C) XP_005249548.1:n.922+2161_922+2162insGGTCCTTGGAGGTACTATACAGTA...
XM_011515000.1:c.922+2161_922+2162insGGTCCTTGGAGGTACTATACAGTATCAAGTATAGTACCTCTAAAGACTG (POLR1C) XP_011513302.1:n.922+2161_922+2162insGGTCCTTGGAGGTACTATACAGTA...
NM_001318876.1:c.922+2161_922+2162insGGTCCTTGGAGGTACTATACAGTATCAAGTATAGTACCTCTAAAGACTG (POLR1C) NP_001305805.1:n.922+2161_922+2162insGGTCCTTGGAGGTACTATACAGTA...
NM_001363658.1:c.922+2161_922+2162insGGTCCTTGGAGGTACTATACAGTATCAAGTATAGTACCTCTAAAGACTG (POLR1C) NP_001350587.1:n.922+2161_922+2162insGGTCCTTGGAGGTACTATACAGTA...
NR_144392.1:n.4622_4623insCAGTCTTTAGAGGTACTATACTTGATACTGTATAGTACCTCCAAGGACC (XPO5)
NM_020750.3:c.*658_*659insCAGTCTTTAGAGGTACTATACTTGATACTGTATAGTACCTCCAAGGACC (XPO5) MANE Select NP_065801.1:n.*658_*659insCAGTCTTTAGAGGTACTATACTTGATACTGTATAG...
NM_001363658.2:c.922+2161_922+2162insGGTCCTTGGAGGTACTATACAGTATCAAGTATAGTACCTCTAAAGACTG (POLR1C) NP_001350587.1:n.922+2161_922+2162insGGTCCTTGGAGGTACTATACAGTA...
NM_001318876.2:c.922+2161_922+2162insGGTCCTTGGAGGTACTATACAGTATCAAGTATAGTACCTCTAAAGACTG (POLR1C) NP_001305805.1:n.922+2161_922+2162insGGTCCTTGGAGGTACTATACAGTA...
NR_144392.2:n.4585_4586insCAGTCTTTAGAGGTACTATACTTGATACTGTATAGTACCTCCAAGGACC (XPO5)