Canonical Allele Identifier: CA143229393

Gene: CNR1

Linked Data

• dbSNP Id: rs945772148
• MyVariant Identifiers: chr6:g.88872736_88872737del (hg19) ; chr6:g.88163017_88163018del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.88163017_88163018del , CM000668.2:g.88163017_88163018del	GRCh38
NC_000006.11:g.88872736_88872737del , CM000668.1:g.88872736_88872737del	GRCh37
NC_000006.10:g.88929455_88929456del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369499.3:c.-64+1239_-64+1240del	ENSP00000358511.2:n.-64+1239_-64+1240del
ENST00000369501.3:c.-64+2785_-64+2786del MANE Select	ENSP00000358513.2:n.-64+2785_-64+2786del
ENST00000428600.3:c.-125_-124del	ENSP00000412192.2:n.-125_-124del
ENST00000551417.2:c.-207+1239_-207+1240del	ENSP00000446702.2:n.-207+1239_-207+1240del
ENST00000369499.2:c.-64+1239_-64+1240del	ENSP00000358511.2:n.-64+1239_-64+1240del
ENST00000369501.2:c.-64+2785_-64+2786del	ENSP00000358513.2:n.-64+2785_-64+2786del
ENST00000428600.2:c.-125_-124del	ENSP00000412192.2:n.-125_-124del
ENST00000551417.1:c.-207+1239_-207+1240del	ENSP00000446702.1:n.-207+1239_-207+1240del
NM_001160226.1:c.-207+2785_-207+2786del	NP_001153698.1:n.-207+2785_-207+2786del
NM_001160258.1:c.-207+1239_-207+1240del	NP_001153730.1:n.-207+1239_-207+1240del
NM_001160259.1:c.-64+2729_-64+2730del	NP_001153731.1:n.-64+2729_-64+2730del
NM_016083.4:c.-64+2785_-64+2786del	NP_057167.2:n.-64+2785_-64+2786del
XM_006715330.2:c.-64+3558_-64+3559del	XP_006715393.1:n.-64+3558_-64+3559del
XM_011535424.1:c.-255+2785_-255+2786del	XP_011533726.1:n.-255+2785_-255+2786del
XM_011535425.1:c.-255+1239_-255+1240del	XP_011533727.1:n.-255+1239_-255+1240del
XM_011535426.1:c.-413+1239_-413+1240del	XP_011533728.1:n.-413+1239_-413+1240del
XM_011535427.1:c.-366+1239_-366+1240del	XP_011533729.1:n.-366+1239_-366+1240del
XM_011535428.1:c.-64+1239_-64+1240del	XP_011533730.1:n.-64+1239_-64+1240del
NM_001160226.2:c.-207+2785_-207+2786del	NP_001153698.1:n.-207+2785_-207+2786del
NM_001160258.2:c.-207+1239_-207+1240del	NP_001153730.1:n.-207+1239_-207+1240del
NM_001160259.2:c.-64+2729_-64+2730del	NP_001153731.1:n.-64+2729_-64+2730del
NM_001365869.1:c.-64+1239_-64+1240del	NP_001352798.1:n.-64+1239_-64+1240del
NM_001365870.1:c.-255+2785_-255+2786del	NP_001352799.1:n.-255+2785_-255+2786del
NM_001365872.1:c.-413+1239_-413+1240del	NP_001352801.1:n.-413+1239_-413+1240del
NM_001365874.1:c.-125_-124del	NP_001352803.1:n.-125_-124del
NM_016083.5:c.-64+2785_-64+2786del	NP_057167.2:n.-64+2785_-64+2786del
XM_006715330.3:c.-64+3558_-64+3559del	XP_006715393.1:n.-64+3558_-64+3559del
XM_011535425.2:c.-255+1239_-255+1240del	XP_011533727.1:n.-255+1239_-255+1240del
XM_017010240.2:c.-64+4172_-64+4173del	XP_016865729.1:n.-64+4172_-64+4173del
NM_001160226.3:c.-207+2785_-207+2786del	NP_001153698.1:n.-207+2785_-207+2786del
NM_001160258.3:c.-207+1239_-207+1240del	NP_001153730.1:n.-207+1239_-207+1240del
NM_001160259.3:c.-64+2729_-64+2730del	NP_001153731.1:n.-64+2729_-64+2730del
NM_001365869.2:c.-64+1239_-64+1240del	NP_001352798.1:n.-64+1239_-64+1240del
NM_001365870.2:c.-255+2785_-255+2786del	NP_001352799.1:n.-255+2785_-255+2786del
NM_001365872.2:c.-413+1239_-413+1240del	NP_001352801.1:n.-413+1239_-413+1240del
NM_001365874.2:c.-125_-124del	NP_001352803.1:n.-125_-124del
NM_001370545.1:c.-64+3558_-64+3559del	NP_001357474.1:n.-64+3558_-64+3559del
NM_001370546.1:c.-64+4172_-64+4173del	NP_001357475.1:n.-64+4172_-64+4173del
NM_001370547.1:c.-255+1239_-255+1240del	NP_001357476.1:n.-255+1239_-255+1240del
NM_016083.6:c.-64+2785_-64+2786del MANE Select	NP_057167.2:n.-64+2785_-64+2786del
NM_001365874.3:c.-125_-124del	NP_001352803.1:n.-125_-124del