Canonical Allele Identifier: CA1644866182
Gene: CNR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.88163126_88163131delinsTCTTAG , CM000668.2:g.88163126_88163131delinsTCTTAG GRCh38
NC_000006.11:g.88872845_88872850delinsTCTTAG , CM000668.1:g.88872845_88872850delinsTCTTAG GRCh37
NC_000006.10:g.88929564_88929569delinsTCTTAG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369499.3:c.-64+1126_-64+1131delinsCTAAGA ENSP00000358511.2:n.-64+1126_-64+1131deli...
ENST00000369501.3:c.-64+2672_-64+2677delinsCTAAGA MANE Select ENSP00000358513.2:n.-64+2672_-64+2677deli...
ENST00000551417.2:c.-207+1126_-207+1131delinsCTAAGA ENSP00000446702.2:n.-207+1126_-207+1131de...
ENST00000369499.2:c.-64+1126_-64+1131delinsCTAAGA ENSP00000358511.2:n.-64+1126_-64+1131deli...
ENST00000369501.2:c.-64+2672_-64+2677delinsCTAAGA ENSP00000358513.2:n.-64+2672_-64+2677deli...
ENST00000551417.1:c.-207+1126_-207+1131delinsCTAAGA ENSP00000446702.1:n.-207+1126_-207+1131de...
NM_001160226.1:c.-207+2672_-207+2677delinsCTAAGA NP_001153698.1:n.-207+2672_-207+2677delin...
NM_001160258.1:c.-207+1126_-207+1131delinsCTAAGA NP_001153730.1:n.-207+1126_-207+1131delin...
NM_001160259.1:c.-64+2616_-64+2621delinsCTAAGA NP_001153731.1:n.-64+2616_-64+2621delinsC...
NM_016083.4:c.-64+2672_-64+2677delinsCTAAGA NP_057167.2:n.-64+2672_-64+2677delinsCTAA...
XM_006715330.2:c.-64+3445_-64+3450delinsCTAAGA XP_006715393.1:n.-64+3445_-64+3450delinsC...
XM_011535424.1:c.-255+2672_-255+2677delinsCTAAGA XP_011533726.1:n.-255+2672_-255+2677delin...
XM_011535425.1:c.-255+1126_-255+1131delinsCTAAGA XP_011533727.1:n.-255+1126_-255+1131delin...
XM_011535426.1:c.-413+1126_-413+1131delinsCTAAGA XP_011533728.1:n.-413+1126_-413+1131delin...
XM_011535427.1:c.-366+1126_-366+1131delinsCTAAGA XP_011533729.1:n.-366+1126_-366+1131delin...
XM_011535428.1:c.-64+1126_-64+1131delinsCTAAGA XP_011533730.1:n.-64+1126_-64+1131delinsC...
NM_001160226.2:c.-207+2672_-207+2677delinsCTAAGA NP_001153698.1:n.-207+2672_-207+2677delin...
NM_001160258.2:c.-207+1126_-207+1131delinsCTAAGA NP_001153730.1:n.-207+1126_-207+1131delin...
NM_001160259.2:c.-64+2616_-64+2621delinsCTAAGA NP_001153731.1:n.-64+2616_-64+2621delinsC...
NM_001365869.1:c.-64+1126_-64+1131delinsCTAAGA NP_001352798.1:n.-64+1126_-64+1131delinsC...
NM_001365870.1:c.-255+2672_-255+2677delinsCTAAGA NP_001352799.1:n.-255+2672_-255+2677delin...
NM_001365872.1:c.-413+1126_-413+1131delinsCTAAGA NP_001352801.1:n.-413+1126_-413+1131delin...
NM_016083.5:c.-64+2672_-64+2677delinsCTAAGA NP_057167.2:n.-64+2672_-64+2677delinsCTAA...
XM_006715330.3:c.-64+3445_-64+3450delinsCTAAGA XP_006715393.1:n.-64+3445_-64+3450delinsC...
XM_011535425.2:c.-255+1126_-255+1131delinsCTAAGA XP_011533727.1:n.-255+1126_-255+1131delin...
XM_017010240.2:c.-64+4059_-64+4064delinsCTAAGA XP_016865729.1:n.-64+4059_-64+4064delinsC...
NM_001160226.3:c.-207+2672_-207+2677delinsCTAAGA NP_001153698.1:n.-207+2672_-207+2677delin...
NM_001160258.3:c.-207+1126_-207+1131delinsCTAAGA NP_001153730.1:n.-207+1126_-207+1131delin...
NM_001160259.3:c.-64+2616_-64+2621delinsCTAAGA NP_001153731.1:n.-64+2616_-64+2621delinsC...
NM_001365869.2:c.-64+1126_-64+1131delinsCTAAGA NP_001352798.1:n.-64+1126_-64+1131delinsC...
NM_001365870.2:c.-255+2672_-255+2677delinsCTAAGA NP_001352799.1:n.-255+2672_-255+2677delin...
NM_001365872.2:c.-413+1126_-413+1131delinsCTAAGA NP_001352801.1:n.-413+1126_-413+1131delin...
NM_001370545.1:c.-64+3445_-64+3450delinsCTAAGA NP_001357474.1:n.-64+3445_-64+3450delinsC...
NM_001370546.1:c.-64+4059_-64+4064delinsCTAAGA NP_001357475.1:n.-64+4059_-64+4064delinsC...
NM_001370547.1:c.-255+1126_-255+1131delinsCTAAGA NP_001357476.1:n.-255+1126_-255+1131delin...
NM_016083.6:c.-64+2672_-64+2677delinsCTAAGA MANE Select NP_057167.2:n.-64+2672_-64+2677delinsCTAA...