Canonical Allele Identifier: CA1091539018

Gene: CNR1

Linked Data

• dbSNP Id: rs1778200257
• gnomAD v3: 6-88163295-CAATTT-C
• gnomAD v4: 6-88163295-CAATTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.88163296_88163300del , CM000668.2:g.88163296_88163300del	GRCh38
NC_000006.11:g.88873015_88873019del , CM000668.1:g.88873015_88873019del	GRCh37
NC_000006.10:g.88929734_88929738del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369499.3:c.-64+957_-64+961del	ENSP00000358511.2:n.-64+957_-64+961del
ENST00000369501.3:c.-64+2503_-64+2507del MANE Select	ENSP00000358513.2:n.-64+2503_-64+2507del
ENST00000551417.2:c.-207+957_-207+961del	ENSP00000446702.2:n.-207+957_-207+961del
ENST00000369499.2:c.-64+957_-64+961del	ENSP00000358511.2:n.-64+957_-64+961del
ENST00000369501.2:c.-64+2503_-64+2507del	ENSP00000358513.2:n.-64+2503_-64+2507del
ENST00000551417.1:c.-207+957_-207+961del	ENSP00000446702.1:n.-207+957_-207+961del
NM_001160226.1:c.-207+2503_-207+2507del	NP_001153698.1:n.-207+2503_-207+2507del
NM_001160258.1:c.-207+957_-207+961del	NP_001153730.1:n.-207+957_-207+961del
NM_001160259.1:c.-64+2447_-64+2451del	NP_001153731.1:n.-64+2447_-64+2451del
NM_016083.4:c.-64+2503_-64+2507del	NP_057167.2:n.-64+2503_-64+2507del
XM_006715330.2:c.-64+3276_-64+3280del	XP_006715393.1:n.-64+3276_-64+3280del
XM_011535424.1:c.-255+2503_-255+2507del	XP_011533726.1:n.-255+2503_-255+2507del
XM_011535425.1:c.-255+957_-255+961del	XP_011533727.1:n.-255+957_-255+961del
XM_011535426.1:c.-413+957_-413+961del	XP_011533728.1:n.-413+957_-413+961del
XM_011535427.1:c.-366+957_-366+961del	XP_011533729.1:n.-366+957_-366+961del
XM_011535428.1:c.-64+957_-64+961del	XP_011533730.1:n.-64+957_-64+961del
NM_001160226.2:c.-207+2503_-207+2507del	NP_001153698.1:n.-207+2503_-207+2507del
NM_001160258.2:c.-207+957_-207+961del	NP_001153730.1:n.-207+957_-207+961del
NM_001160259.2:c.-64+2447_-64+2451del	NP_001153731.1:n.-64+2447_-64+2451del
NM_001365869.1:c.-64+957_-64+961del	NP_001352798.1:n.-64+957_-64+961del
NM_001365870.1:c.-255+2503_-255+2507del	NP_001352799.1:n.-255+2503_-255+2507del
NM_001365872.1:c.-413+957_-413+961del	NP_001352801.1:n.-413+957_-413+961del
NM_016083.5:c.-64+2503_-64+2507del	NP_057167.2:n.-64+2503_-64+2507del
XM_006715330.3:c.-64+3276_-64+3280del	XP_006715393.1:n.-64+3276_-64+3280del
XM_011535425.2:c.-255+957_-255+961del	XP_011533727.1:n.-255+957_-255+961del
XM_017010240.2:c.-64+3890_-64+3894del	XP_016865729.1:n.-64+3890_-64+3894del
NM_001160226.3:c.-207+2503_-207+2507del	NP_001153698.1:n.-207+2503_-207+2507del
NM_001160258.3:c.-207+957_-207+961del	NP_001153730.1:n.-207+957_-207+961del
NM_001160259.3:c.-64+2447_-64+2451del	NP_001153731.1:n.-64+2447_-64+2451del
NM_001365869.2:c.-64+957_-64+961del	NP_001352798.1:n.-64+957_-64+961del
NM_001365870.2:c.-255+2503_-255+2507del	NP_001352799.1:n.-255+2503_-255+2507del
NM_001365872.2:c.-413+957_-413+961del	NP_001352801.1:n.-413+957_-413+961del
NM_001370545.1:c.-64+3276_-64+3280del	NP_001357474.1:n.-64+3276_-64+3280del
NM_001370546.1:c.-64+3890_-64+3894del	NP_001357475.1:n.-64+3890_-64+3894del
NM_001370547.1:c.-255+957_-255+961del	NP_001357476.1:n.-255+957_-255+961del
NM_016083.6:c.-64+2503_-64+2507del MANE Select	NP_057167.2:n.-64+2503_-64+2507del