Canonical Allele Identifier: CA1091535527

Gene: CNR1

Linked Data

• dbSNP Id: rs1777680542
• gnomAD v3: 6-88154279-CA-C
• gnomAD v4: 6-88154279-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.88154282del , CM000668.2:g.88154282del	GRCh38
NC_000006.11:g.88864001del , CM000668.1:g.88864001del	GRCh37
NC_000006.10:g.88920720del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369499.3:c.-63-8943del	ENSP00000358511.2:n.-63-8943del
ENST00000369501.3:c.-63-8943del MANE Select	ENSP00000358513.2:n.-63-8943del
ENST00000428600.3:c.-64+8677del	ENSP00000412192.2:n.-64+8677del
ENST00000551417.2:c.-206-6474del	ENSP00000446702.2:n.-206-6474del
ENST00000369499.2:c.-63-8943del	ENSP00000358511.2:n.-63-8943del
ENST00000369501.2:c.-63-8943del	ENSP00000358513.2:n.-63-8943del
ENST00000428600.2:c.-64+8677del	ENSP00000412192.2:n.-64+8677del
ENST00000551417.1:c.-206-6474del	ENSP00000446702.1:n.-206-6474del
NM_001160226.1:c.-206-6474del	NP_001153698.1:n.-206-6474del
NM_001160258.1:c.-206-6474del	NP_001153730.1:n.-206-6474del
NM_001160259.1:c.-63-8943del	NP_001153731.1:n.-63-8943del
NM_016083.4:c.-63-8943del	NP_057167.2:n.-63-8943del
XM_006715330.2:c.-63-8943del	XP_006715393.1:n.-63-8943del
XM_011535424.1:c.-254-6474del	XP_011533726.1:n.-254-6474del
XM_011535425.1:c.-254-6474del	XP_011533727.1:n.-254-6474del
XM_011535426.1:c.-412-3640del	XP_011533728.1:n.-412-3640del
XM_011535427.1:c.-365-3687del	XP_011533729.1:n.-365-3687del
XM_011535428.1:c.-63-8943del	XP_011533730.1:n.-63-8943del
NM_001160226.2:c.-206-6474del	NP_001153698.1:n.-206-6474del
NM_001160258.2:c.-206-6474del	NP_001153730.1:n.-206-6474del
NM_001160259.2:c.-63-8943del	NP_001153731.1:n.-63-8943del
NM_001365869.1:c.-63-8943del	NP_001352798.1:n.-63-8943del
NM_001365870.1:c.-254-6474del	NP_001352799.1:n.-254-6474del
NM_001365872.1:c.-412-3640del	NP_001352801.1:n.-412-3640del
NM_001365874.1:c.-64+8677del	NP_001352803.1:n.-64+8677del
NM_016083.5:c.-63-8943del	NP_057167.2:n.-63-8943del
XM_006715330.3:c.-63-8943del	XP_006715393.1:n.-63-8943del
XM_011535425.2:c.-254-6474del	XP_011533727.1:n.-254-6474del
XM_017010240.2:c.-63-8943del	XP_016865729.1:n.-63-8943del
NM_001160226.3:c.-206-6474del	NP_001153698.1:n.-206-6474del
NM_001160258.3:c.-206-6474del	NP_001153730.1:n.-206-6474del
NM_001160259.3:c.-63-8943del	NP_001153731.1:n.-63-8943del
NM_001365869.2:c.-63-8943del	NP_001352798.1:n.-63-8943del
NM_001365870.2:c.-254-6474del	NP_001352799.1:n.-254-6474del
NM_001365872.2:c.-412-3640del	NP_001352801.1:n.-412-3640del
NM_001365874.2:c.-64+8677del	NP_001352803.1:n.-64+8677del
NM_001370545.1:c.-63-8943del	NP_001357474.1:n.-63-8943del
NM_001370546.1:c.-63-8943del	NP_001357475.1:n.-63-8943del
NM_001370547.1:c.-254-6474del	NP_001357476.1:n.-254-6474del
NM_016083.6:c.-63-8943del MANE Select	NP_057167.2:n.-63-8943del
NM_001365874.3:c.-64+8677del	NP_001352803.1:n.-64+8677del