Canonical Allele Identifier: CA1644866250
Gene: CNR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.88163295_88163300delinsCAATTT , CM000668.2:g.88163295_88163300delinsCAATTT GRCh38
NC_000006.11:g.88873014_88873019delinsCAATTT , CM000668.1:g.88873014_88873019delinsCAATTT GRCh37
NC_000006.10:g.88929733_88929738delinsCAATTT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369499.3:c.-64+957_-64+962delinsAAATTG ENSP00000358511.2:n.-64+957_-64+962delins...
ENST00000369501.3:c.-64+2503_-64+2508delinsAAATTG MANE Select ENSP00000358513.2:n.-64+2503_-64+2508deli...
ENST00000551417.2:c.-207+957_-207+962delinsAAATTG ENSP00000446702.2:n.-207+957_-207+962deli...
ENST00000369499.2:c.-64+957_-64+962delinsAAATTG ENSP00000358511.2:n.-64+957_-64+962delins...
ENST00000369501.2:c.-64+2503_-64+2508delinsAAATTG ENSP00000358513.2:n.-64+2503_-64+2508deli...
ENST00000551417.1:c.-207+957_-207+962delinsAAATTG ENSP00000446702.1:n.-207+957_-207+962deli...
NM_001160226.1:c.-207+2503_-207+2508delinsAAATTG NP_001153698.1:n.-207+2503_-207+2508delin...
NM_001160258.1:c.-207+957_-207+962delinsAAATTG NP_001153730.1:n.-207+957_-207+962delinsA...
NM_001160259.1:c.-64+2447_-64+2452delinsAAATTG NP_001153731.1:n.-64+2447_-64+2452delinsA...
NM_016083.4:c.-64+2503_-64+2508delinsAAATTG NP_057167.2:n.-64+2503_-64+2508delinsAAAT...
XM_006715330.2:c.-64+3276_-64+3281delinsAAATTG XP_006715393.1:n.-64+3276_-64+3281delinsA...
XM_011535424.1:c.-255+2503_-255+2508delinsAAATTG XP_011533726.1:n.-255+2503_-255+2508delin...
XM_011535425.1:c.-255+957_-255+962delinsAAATTG XP_011533727.1:n.-255+957_-255+962delinsA...
XM_011535426.1:c.-413+957_-413+962delinsAAATTG XP_011533728.1:n.-413+957_-413+962delinsA...
XM_011535427.1:c.-366+957_-366+962delinsAAATTG XP_011533729.1:n.-366+957_-366+962delinsA...
XM_011535428.1:c.-64+957_-64+962delinsAAATTG XP_011533730.1:n.-64+957_-64+962delinsAAA...
NM_001160226.2:c.-207+2503_-207+2508delinsAAATTG NP_001153698.1:n.-207+2503_-207+2508delin...
NM_001160258.2:c.-207+957_-207+962delinsAAATTG NP_001153730.1:n.-207+957_-207+962delinsA...
NM_001160259.2:c.-64+2447_-64+2452delinsAAATTG NP_001153731.1:n.-64+2447_-64+2452delinsA...
NM_001365869.1:c.-64+957_-64+962delinsAAATTG NP_001352798.1:n.-64+957_-64+962delinsAAA...
NM_001365870.1:c.-255+2503_-255+2508delinsAAATTG NP_001352799.1:n.-255+2503_-255+2508delin...
NM_001365872.1:c.-413+957_-413+962delinsAAATTG NP_001352801.1:n.-413+957_-413+962delinsA...
NM_016083.5:c.-64+2503_-64+2508delinsAAATTG NP_057167.2:n.-64+2503_-64+2508delinsAAAT...
XM_006715330.3:c.-64+3276_-64+3281delinsAAATTG XP_006715393.1:n.-64+3276_-64+3281delinsA...
XM_011535425.2:c.-255+957_-255+962delinsAAATTG XP_011533727.1:n.-255+957_-255+962delinsA...
XM_017010240.2:c.-64+3890_-64+3895delinsAAATTG XP_016865729.1:n.-64+3890_-64+3895delinsA...
NM_001160226.3:c.-207+2503_-207+2508delinsAAATTG NP_001153698.1:n.-207+2503_-207+2508delin...
NM_001160258.3:c.-207+957_-207+962delinsAAATTG NP_001153730.1:n.-207+957_-207+962delinsA...
NM_001160259.3:c.-64+2447_-64+2452delinsAAATTG NP_001153731.1:n.-64+2447_-64+2452delinsA...
NM_001365869.2:c.-64+957_-64+962delinsAAATTG NP_001352798.1:n.-64+957_-64+962delinsAAA...
NM_001365870.2:c.-255+2503_-255+2508delinsAAATTG NP_001352799.1:n.-255+2503_-255+2508delin...
NM_001365872.2:c.-413+957_-413+962delinsAAATTG NP_001352801.1:n.-413+957_-413+962delinsA...
NM_001370545.1:c.-64+3276_-64+3281delinsAAATTG NP_001357474.1:n.-64+3276_-64+3281delinsA...
NM_001370546.1:c.-64+3890_-64+3895delinsAAATTG NP_001357475.1:n.-64+3890_-64+3895delinsA...
NM_001370547.1:c.-255+957_-255+962delinsAAATTG NP_001357476.1:n.-255+957_-255+962delinsA...
NM_016083.6:c.-64+2503_-64+2508delinsAAATTG MANE Select NP_057167.2:n.-64+2503_-64+2508delinsAAAT...