Canonical Allele Identifier: CA1644866161

Gene: CNR1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.88163089_88163093delinsTTTAA , CM000668.2:g.88163089_88163093delinsTTTAA	GRCh38
NC_000006.11:g.88872808_88872812delinsTTTAA , CM000668.1:g.88872808_88872812delinsTTTAA	GRCh37
NC_000006.10:g.88929527_88929531delinsTTTAA	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369499.3:c.-64+1164_-64+1168delinsTTAAA	ENSP00000358511.2:n.-64+1164_-64+1168deli...
ENST00000369501.3:c.-64+2710_-64+2714delinsTTAAA MANE Select	ENSP00000358513.2:n.-64+2710_-64+2714deli...
ENST00000551417.2:c.-207+1164_-207+1168delinsTTAAA	ENSP00000446702.2:n.-207+1164_-207+1168de...
ENST00000369499.2:c.-64+1164_-64+1168delinsTTAAA	ENSP00000358511.2:n.-64+1164_-64+1168deli...
ENST00000369501.2:c.-64+2710_-64+2714delinsTTAAA	ENSP00000358513.2:n.-64+2710_-64+2714deli...
ENST00000551417.1:c.-207+1164_-207+1168delinsTTAAA	ENSP00000446702.1:n.-207+1164_-207+1168de...
NM_001160226.1:c.-207+2710_-207+2714delinsTTAAA	NP_001153698.1:n.-207+2710_-207+2714delin...
NM_001160258.1:c.-207+1164_-207+1168delinsTTAAA	NP_001153730.1:n.-207+1164_-207+1168delin...
NM_001160259.1:c.-64+2654_-64+2658delinsTTAAA	NP_001153731.1:n.-64+2654_-64+2658delinsT...
NM_016083.4:c.-64+2710_-64+2714delinsTTAAA	NP_057167.2:n.-64+2710_-64+2714delinsTTAA...
XM_006715330.2:c.-64+3483_-64+3487delinsTTAAA	XP_006715393.1:n.-64+3483_-64+3487delinsT...
XM_011535424.1:c.-255+2710_-255+2714delinsTTAAA	XP_011533726.1:n.-255+2710_-255+2714delin...
XM_011535425.1:c.-255+1164_-255+1168delinsTTAAA	XP_011533727.1:n.-255+1164_-255+1168delin...
XM_011535426.1:c.-413+1164_-413+1168delinsTTAAA	XP_011533728.1:n.-413+1164_-413+1168delin...
XM_011535427.1:c.-366+1164_-366+1168delinsTTAAA	XP_011533729.1:n.-366+1164_-366+1168delin...
XM_011535428.1:c.-64+1164_-64+1168delinsTTAAA	XP_011533730.1:n.-64+1164_-64+1168delinsT...
NM_001160226.2:c.-207+2710_-207+2714delinsTTAAA	NP_001153698.1:n.-207+2710_-207+2714delin...
NM_001160258.2:c.-207+1164_-207+1168delinsTTAAA	NP_001153730.1:n.-207+1164_-207+1168delin...
NM_001160259.2:c.-64+2654_-64+2658delinsTTAAA	NP_001153731.1:n.-64+2654_-64+2658delinsT...
NM_001365869.1:c.-64+1164_-64+1168delinsTTAAA	NP_001352798.1:n.-64+1164_-64+1168delinsT...
NM_001365870.1:c.-255+2710_-255+2714delinsTTAAA	NP_001352799.1:n.-255+2710_-255+2714delin...
NM_001365872.1:c.-413+1164_-413+1168delinsTTAAA	NP_001352801.1:n.-413+1164_-413+1168delin...
NM_001365874.1:c.-200_-196delinsTTAAA	NP_001352803.1:n.-200_-196delinsTTAAA
NM_016083.5:c.-64+2710_-64+2714delinsTTAAA	NP_057167.2:n.-64+2710_-64+2714delinsTTAA...
XM_006715330.3:c.-64+3483_-64+3487delinsTTAAA	XP_006715393.1:n.-64+3483_-64+3487delinsT...
XM_011535425.2:c.-255+1164_-255+1168delinsTTAAA	XP_011533727.1:n.-255+1164_-255+1168delin...
XM_017010240.2:c.-64+4097_-64+4101delinsTTAAA	XP_016865729.1:n.-64+4097_-64+4101delinsT...
NM_001160226.3:c.-207+2710_-207+2714delinsTTAAA	NP_001153698.1:n.-207+2710_-207+2714delin...
NM_001160258.3:c.-207+1164_-207+1168delinsTTAAA	NP_001153730.1:n.-207+1164_-207+1168delin...
NM_001160259.3:c.-64+2654_-64+2658delinsTTAAA	NP_001153731.1:n.-64+2654_-64+2658delinsT...
NM_001365869.2:c.-64+1164_-64+1168delinsTTAAA	NP_001352798.1:n.-64+1164_-64+1168delinsT...
NM_001365870.2:c.-255+2710_-255+2714delinsTTAAA	NP_001352799.1:n.-255+2710_-255+2714delin...
NM_001365872.2:c.-413+1164_-413+1168delinsTTAAA	NP_001352801.1:n.-413+1164_-413+1168delin...
NM_001370545.1:c.-64+3483_-64+3487delinsTTAAA	NP_001357474.1:n.-64+3483_-64+3487delinsT...
NM_001370546.1:c.-64+4097_-64+4101delinsTTAAA	NP_001357475.1:n.-64+4097_-64+4101delinsT...
NM_001370547.1:c.-255+1164_-255+1168delinsTTAAA	NP_001357476.1:n.-255+1164_-255+1168delin...
NM_016083.6:c.-64+2710_-64+2714delinsTTAAA MANE Select	NP_057167.2:n.-64+2710_-64+2714delinsTTAA...