Canonical Allele Identifier: CA829361816

Gene: CNR1

Linked Data

• dbSNP Id: rs1400555837
• gnomAD v3: 6-88154964-T-TA
• gnomAD v4: 6-88154964-T-TA
• MyVariant Identifiers: chr6:g.88864683_88864684insA (hg19) ; chr6:g.88154964_88154965insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.88154965dup , CM000668.2:g.88154965dup	GRCh38
NC_000006.11:g.88864684dup , CM000668.1:g.88864684dup	GRCh37
NC_000006.10:g.88921403dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369499.3:c.-64+9292dup	ENSP00000358511.2:n.-64+9292dup
ENST00000369501.3:c.-63-9628dup MANE Select	ENSP00000358513.2:n.-63-9628dup
ENST00000428600.3:c.-64+7992dup	ENSP00000412192.2:n.-64+7992dup
ENST00000551417.2:c.-206-7159dup	ENSP00000446702.2:n.-206-7159dup
ENST00000369499.2:c.-64+9292dup	ENSP00000358511.2:n.-64+9292dup
ENST00000369501.2:c.-63-9628dup	ENSP00000358513.2:n.-63-9628dup
ENST00000428600.2:c.-64+7992dup	ENSP00000412192.2:n.-64+7992dup
ENST00000551417.1:c.-206-7159dup	ENSP00000446702.1:n.-206-7159dup
NM_001160226.1:c.-206-7159dup	NP_001153698.1:n.-206-7159dup
NM_001160258.1:c.-206-7159dup	NP_001153730.1:n.-206-7159dup
NM_001160259.1:c.-63-9628dup	NP_001153731.1:n.-63-9628dup
NM_016083.4:c.-63-9628dup	NP_057167.2:n.-63-9628dup
XM_006715330.2:c.-63-9628dup	XP_006715393.1:n.-63-9628dup
XM_011535424.1:c.-254-7159dup	XP_011533726.1:n.-254-7159dup
XM_011535425.1:c.-254-7159dup	XP_011533727.1:n.-254-7159dup
XM_011535426.1:c.-412-4325dup	XP_011533728.1:n.-412-4325dup
XM_011535427.1:c.-365-4372dup	XP_011533729.1:n.-365-4372dup
XM_011535428.1:c.-64+9292dup	XP_011533730.1:n.-64+9292dup
NM_001160226.2:c.-206-7159dup	NP_001153698.1:n.-206-7159dup
NM_001160258.2:c.-206-7159dup	NP_001153730.1:n.-206-7159dup
NM_001160259.2:c.-63-9628dup	NP_001153731.1:n.-63-9628dup
NM_001365869.1:c.-64+9292dup	NP_001352798.1:n.-64+9292dup
NM_001365870.1:c.-254-7159dup	NP_001352799.1:n.-254-7159dup
NM_001365872.1:c.-412-4325dup	NP_001352801.1:n.-412-4325dup
NM_001365874.1:c.-64+7992dup	NP_001352803.1:n.-64+7992dup
NM_016083.5:c.-63-9628dup	NP_057167.2:n.-63-9628dup
XM_006715330.3:c.-63-9628dup	XP_006715393.1:n.-63-9628dup
XM_011535425.2:c.-254-7159dup	XP_011533727.1:n.-254-7159dup
XM_017010240.2:c.-63-9628dup	XP_016865729.1:n.-63-9628dup
NM_001160226.3:c.-206-7159dup	NP_001153698.1:n.-206-7159dup
NM_001160258.3:c.-206-7159dup	NP_001153730.1:n.-206-7159dup
NM_001160259.3:c.-63-9628dup	NP_001153731.1:n.-63-9628dup
NM_001365869.2:c.-64+9292dup	NP_001352798.1:n.-64+9292dup
NM_001365870.2:c.-254-7159dup	NP_001352799.1:n.-254-7159dup
NM_001365872.2:c.-412-4325dup	NP_001352801.1:n.-412-4325dup
NM_001365874.2:c.-64+7992dup	NP_001352803.1:n.-64+7992dup
NM_001370545.1:c.-63-9628dup	NP_001357474.1:n.-63-9628dup
NM_001370546.1:c.-63-9628dup	NP_001357475.1:n.-63-9628dup
NM_001370547.1:c.-254-7159dup	NP_001357476.1:n.-254-7159dup
NM_016083.6:c.-63-9628dup MANE Select	NP_057167.2:n.-63-9628dup
NM_001365874.3:c.-64+7992dup	NP_001352803.1:n.-64+7992dup