Canonical Allele Identifier: CA1644866184
Gene: CNR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.88163127_88163128delinsCT , CM000668.2:g.88163127_88163128delinsCT GRCh38
NC_000006.11:g.88872846_88872847delinsCT , CM000668.1:g.88872846_88872847delinsCT GRCh37
NC_000006.10:g.88929565_88929566delinsCT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369499.3:c.-64+1129_-64+1130delinsAG ENSP00000358511.2:n.-64+1129_-64+1130deli...
ENST00000369501.3:c.-64+2675_-64+2676delinsAG MANE Select ENSP00000358513.2:n.-64+2675_-64+2676deli...
ENST00000551417.2:c.-207+1129_-207+1130delinsAG ENSP00000446702.2:n.-207+1129_-207+1130de...
ENST00000369499.2:c.-64+1129_-64+1130delinsAG ENSP00000358511.2:n.-64+1129_-64+1130deli...
ENST00000369501.2:c.-64+2675_-64+2676delinsAG ENSP00000358513.2:n.-64+2675_-64+2676deli...
ENST00000551417.1:c.-207+1129_-207+1130delinsAG ENSP00000446702.1:n.-207+1129_-207+1130de...
NM_001160226.1:c.-207+2675_-207+2676delinsAG NP_001153698.1:n.-207+2675_-207+2676delin...
NM_001160258.1:c.-207+1129_-207+1130delinsAG NP_001153730.1:n.-207+1129_-207+1130delin...
NM_001160259.1:c.-64+2619_-64+2620delinsAG NP_001153731.1:n.-64+2619_-64+2620delinsA...
NM_016083.4:c.-64+2675_-64+2676delinsAG NP_057167.2:n.-64+2675_-64+2676delinsAG
XM_006715330.2:c.-64+3448_-64+3449delinsAG XP_006715393.1:n.-64+3448_-64+3449delinsA...
XM_011535424.1:c.-255+2675_-255+2676delinsAG XP_011533726.1:n.-255+2675_-255+2676delin...
XM_011535425.1:c.-255+1129_-255+1130delinsAG XP_011533727.1:n.-255+1129_-255+1130delin...
XM_011535426.1:c.-413+1129_-413+1130delinsAG XP_011533728.1:n.-413+1129_-413+1130delin...
XM_011535427.1:c.-366+1129_-366+1130delinsAG XP_011533729.1:n.-366+1129_-366+1130delin...
XM_011535428.1:c.-64+1129_-64+1130delinsAG XP_011533730.1:n.-64+1129_-64+1130delinsA...
NM_001160226.2:c.-207+2675_-207+2676delinsAG NP_001153698.1:n.-207+2675_-207+2676delin...
NM_001160258.2:c.-207+1129_-207+1130delinsAG NP_001153730.1:n.-207+1129_-207+1130delin...
NM_001160259.2:c.-64+2619_-64+2620delinsAG NP_001153731.1:n.-64+2619_-64+2620delinsA...
NM_001365869.1:c.-64+1129_-64+1130delinsAG NP_001352798.1:n.-64+1129_-64+1130delinsA...
NM_001365870.1:c.-255+2675_-255+2676delinsAG NP_001352799.1:n.-255+2675_-255+2676delin...
NM_001365872.1:c.-413+1129_-413+1130delinsAG NP_001352801.1:n.-413+1129_-413+1130delin...
NM_016083.5:c.-64+2675_-64+2676delinsAG NP_057167.2:n.-64+2675_-64+2676delinsAG
XM_006715330.3:c.-64+3448_-64+3449delinsAG XP_006715393.1:n.-64+3448_-64+3449delinsA...
XM_011535425.2:c.-255+1129_-255+1130delinsAG XP_011533727.1:n.-255+1129_-255+1130delin...
XM_017010240.2:c.-64+4062_-64+4063delinsAG XP_016865729.1:n.-64+4062_-64+4063delinsA...
NM_001160226.3:c.-207+2675_-207+2676delinsAG NP_001153698.1:n.-207+2675_-207+2676delin...
NM_001160258.3:c.-207+1129_-207+1130delinsAG NP_001153730.1:n.-207+1129_-207+1130delin...
NM_001160259.3:c.-64+2619_-64+2620delinsAG NP_001153731.1:n.-64+2619_-64+2620delinsA...
NM_001365869.2:c.-64+1129_-64+1130delinsAG NP_001352798.1:n.-64+1129_-64+1130delinsA...
NM_001365870.2:c.-255+2675_-255+2676delinsAG NP_001352799.1:n.-255+2675_-255+2676delin...
NM_001365872.2:c.-413+1129_-413+1130delinsAG NP_001352801.1:n.-413+1129_-413+1130delin...
NM_001370545.1:c.-64+3448_-64+3449delinsAG NP_001357474.1:n.-64+3448_-64+3449delinsA...
NM_001370546.1:c.-64+4062_-64+4063delinsAG NP_001357475.1:n.-64+4062_-64+4063delinsA...
NM_001370547.1:c.-255+1129_-255+1130delinsAG NP_001357476.1:n.-255+1129_-255+1130delin...
NM_016083.6:c.-64+2675_-64+2676delinsAG MANE Select NP_057167.2:n.-64+2675_-64+2676delinsAG