Canonical Allele Identifier: CA2712629427

Gene: CNR1

Linked Data

• dbSNP Id: rs2127771998

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.88163047_88163050del , CM000668.2:g.88163047_88163050del	GRCh38
NC_000006.11:g.88872766_88872769del , CM000668.1:g.88872766_88872769del	GRCh37
NC_000006.10:g.88929485_88929488del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369499.3:c.-64+1212_-64+1215del	ENSP00000358511.2:n.-64+1212_-64+1215del
ENST00000369501.3:c.-64+2758_-64+2761del MANE Select	ENSP00000358513.2:n.-64+2758_-64+2761del
ENST00000551417.2:c.-207+1212_-207+1215del	ENSP00000446702.2:n.-207+1212_-207+1215del
ENST00000369499.2:c.-64+1212_-64+1215del	ENSP00000358511.2:n.-64+1212_-64+1215del
ENST00000369501.2:c.-64+2758_-64+2761del	ENSP00000358513.2:n.-64+2758_-64+2761del
ENST00000551417.1:c.-207+1212_-207+1215del	ENSP00000446702.1:n.-207+1212_-207+1215del
NM_001160226.1:c.-207+2758_-207+2761del	NP_001153698.1:n.-207+2758_-207+2761del
NM_001160258.1:c.-207+1212_-207+1215del	NP_001153730.1:n.-207+1212_-207+1215del
NM_001160259.1:c.-64+2702_-64+2705del	NP_001153731.1:n.-64+2702_-64+2705del
NM_016083.4:c.-64+2758_-64+2761del	NP_057167.2:n.-64+2758_-64+2761del
XM_006715330.2:c.-64+3531_-64+3534del	XP_006715393.1:n.-64+3531_-64+3534del
XM_011535424.1:c.-255+2758_-255+2761del	XP_011533726.1:n.-255+2758_-255+2761del
XM_011535425.1:c.-255+1212_-255+1215del	XP_011533727.1:n.-255+1212_-255+1215del
XM_011535426.1:c.-413+1212_-413+1215del	XP_011533728.1:n.-413+1212_-413+1215del
XM_011535427.1:c.-366+1212_-366+1215del	XP_011533729.1:n.-366+1212_-366+1215del
XM_011535428.1:c.-64+1212_-64+1215del	XP_011533730.1:n.-64+1212_-64+1215del
NM_001160226.2:c.-207+2758_-207+2761del	NP_001153698.1:n.-207+2758_-207+2761del
NM_001160258.2:c.-207+1212_-207+1215del	NP_001153730.1:n.-207+1212_-207+1215del
NM_001160259.2:c.-64+2702_-64+2705del	NP_001153731.1:n.-64+2702_-64+2705del
NM_001365869.1:c.-64+1212_-64+1215del	NP_001352798.1:n.-64+1212_-64+1215del
NM_001365870.1:c.-255+2758_-255+2761del	NP_001352799.1:n.-255+2758_-255+2761del
NM_001365872.1:c.-413+1212_-413+1215del	NP_001352801.1:n.-413+1212_-413+1215del
NM_001365874.1:c.-152_-149del	NP_001352803.1:n.-152_-149del
NM_016083.5:c.-64+2758_-64+2761del	NP_057167.2:n.-64+2758_-64+2761del
XM_006715330.3:c.-64+3531_-64+3534del	XP_006715393.1:n.-64+3531_-64+3534del
XM_011535425.2:c.-255+1212_-255+1215del	XP_011533727.1:n.-255+1212_-255+1215del
XM_017010240.2:c.-64+4145_-64+4148del	XP_016865729.1:n.-64+4145_-64+4148del
NM_001160226.3:c.-207+2758_-207+2761del	NP_001153698.1:n.-207+2758_-207+2761del
NM_001160258.3:c.-207+1212_-207+1215del	NP_001153730.1:n.-207+1212_-207+1215del
NM_001160259.3:c.-64+2702_-64+2705del	NP_001153731.1:n.-64+2702_-64+2705del
NM_001365869.2:c.-64+1212_-64+1215del	NP_001352798.1:n.-64+1212_-64+1215del
NM_001365870.2:c.-255+2758_-255+2761del	NP_001352799.1:n.-255+2758_-255+2761del
NM_001365872.2:c.-413+1212_-413+1215del	NP_001352801.1:n.-413+1212_-413+1215del
NM_001370545.1:c.-64+3531_-64+3534del	NP_001357474.1:n.-64+3531_-64+3534del
NM_001370546.1:c.-64+4145_-64+4148del	NP_001357475.1:n.-64+4145_-64+4148del
NM_001370547.1:c.-255+1212_-255+1215del	NP_001357476.1:n.-255+1212_-255+1215del
NM_016083.6:c.-64+2758_-64+2761del MANE Select	NP_057167.2:n.-64+2758_-64+2761del