Canonical Allele Identifier: CA568833097

Gene: CNR1

Linked Data

• dbSNP Id: rs1286345018
• gnomAD v2: 6-88861496-G-GAT
• gnomAD v3: 6-88151777-G-GAT
• gnomAD v4: 6-88151777-G-GAT
• MyVariant Identifiers: chr6:g.88861496_88861497insAT (hg19) ; chr6:g.88151777_88151778insAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.88151785_88151786dup , CM000668.2:g.88151785_88151786dup	GRCh38
NC_000006.11:g.88861504_88861505dup , CM000668.1:g.88861504_88861505dup	GRCh37
NC_000006.10:g.88918223_88918224dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369499.3:c.-63-6442_-63-6441dup	ENSP00000358511.2:n.-63-6442_-63-6441dup
ENST00000369501.3:c.-63-6442_-63-6441dup MANE Select	ENSP00000358513.2:n.-63-6442_-63-6441dup
ENST00000428600.3:c.-63-6442_-63-6441dup	ENSP00000412192.2:n.-63-6442_-63-6441dup
ENST00000551417.2:c.-206-3973_-206-3972dup	ENSP00000446702.2:n.-206-3973_-206-3972dup
ENST00000369499.2:c.-63-6442_-63-6441dup	ENSP00000358511.2:n.-63-6442_-63-6441dup
ENST00000369501.2:c.-63-6442_-63-6441dup	ENSP00000358513.2:n.-63-6442_-63-6441dup
ENST00000428600.2:c.-63-6442_-63-6441dup	ENSP00000412192.2:n.-63-6442_-63-6441dup
ENST00000551417.1:c.-206-3973_-206-3972dup	ENSP00000446702.1:n.-206-3973_-206-3972dup
NM_001160226.1:c.-206-3973_-206-3972dup	NP_001153698.1:n.-206-3973_-206-3972dup
NM_001160258.1:c.-206-3973_-206-3972dup	NP_001153730.1:n.-206-3973_-206-3972dup
NM_001160259.1:c.-63-6442_-63-6441dup	NP_001153731.1:n.-63-6442_-63-6441dup
NM_016083.4:c.-63-6442_-63-6441dup	NP_057167.2:n.-63-6442_-63-6441dup
XM_006715330.2:c.-63-6442_-63-6441dup	XP_006715393.1:n.-63-6442_-63-6441dup
XM_011535424.1:c.-254-3973_-254-3972dup	XP_011533726.1:n.-254-3973_-254-3972dup
XM_011535425.1:c.-254-3973_-254-3972dup	XP_011533727.1:n.-254-3973_-254-3972dup
XM_011535426.1:c.-412-1139_-412-1138dup	XP_011533728.1:n.-412-1139_-412-1138dup
XM_011535427.1:c.-365-1186_-365-1185dup	XP_011533729.1:n.-365-1186_-365-1185dup
XM_011535428.1:c.-63-6442_-63-6441dup	XP_011533730.1:n.-63-6442_-63-6441dup
NM_001160226.2:c.-206-3973_-206-3972dup	NP_001153698.1:n.-206-3973_-206-3972dup
NM_001160258.2:c.-206-3973_-206-3972dup	NP_001153730.1:n.-206-3973_-206-3972dup
NM_001160259.2:c.-63-6442_-63-6441dup	NP_001153731.1:n.-63-6442_-63-6441dup
NM_001365869.1:c.-63-6442_-63-6441dup	NP_001352798.1:n.-63-6442_-63-6441dup
NM_001365870.1:c.-254-3973_-254-3972dup	NP_001352799.1:n.-254-3973_-254-3972dup
NM_001365872.1:c.-412-1139_-412-1138dup	NP_001352801.1:n.-412-1139_-412-1138dup
NM_001365874.1:c.-63-6442_-63-6441dup	NP_001352803.1:n.-63-6442_-63-6441dup
NM_016083.5:c.-63-6442_-63-6441dup	NP_057167.2:n.-63-6442_-63-6441dup
XM_006715330.3:c.-63-6442_-63-6441dup	XP_006715393.1:n.-63-6442_-63-6441dup
XM_011535425.2:c.-254-3973_-254-3972dup	XP_011533727.1:n.-254-3973_-254-3972dup
XM_017010240.2:c.-63-6442_-63-6441dup	XP_016865729.1:n.-63-6442_-63-6441dup
NM_001160226.3:c.-206-3973_-206-3972dup	NP_001153698.1:n.-206-3973_-206-3972dup
NM_001160258.3:c.-206-3973_-206-3972dup	NP_001153730.1:n.-206-3973_-206-3972dup
NM_001160259.3:c.-63-6442_-63-6441dup	NP_001153731.1:n.-63-6442_-63-6441dup
NM_001365869.2:c.-63-6442_-63-6441dup	NP_001352798.1:n.-63-6442_-63-6441dup
NM_001365870.2:c.-254-3973_-254-3972dup	NP_001352799.1:n.-254-3973_-254-3972dup
NM_001365872.2:c.-412-1139_-412-1138dup	NP_001352801.1:n.-412-1139_-412-1138dup
NM_001365874.2:c.-63-6442_-63-6441dup	NP_001352803.1:n.-63-6442_-63-6441dup
NM_001370545.1:c.-63-6442_-63-6441dup	NP_001357474.1:n.-63-6442_-63-6441dup
NM_001370546.1:c.-63-6442_-63-6441dup	NP_001357475.1:n.-63-6442_-63-6441dup
NM_001370547.1:c.-254-3973_-254-3972dup	NP_001357476.1:n.-254-3973_-254-3972dup
NM_016083.6:c.-63-6442_-63-6441dup MANE Select	NP_057167.2:n.-63-6442_-63-6441dup
NM_001365874.3:c.-63-6442_-63-6441dup	NP_001352803.1:n.-63-6442_-63-6441dup