Canonical Allele Identifier: CA1091539024

Gene: CNR1

Linked Data

• dbSNP Id: rs1778202147
• gnomAD v3: 6-88163330-T-TGGGAA
• gnomAD v4: 6-88163330-T-TGGGAA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.88163330_88163331insGGGAA , CM000668.2:g.88163330_88163331insGGGAA	GRCh38
NC_000006.11:g.88873049_88873050insGGGAA , CM000668.1:g.88873049_88873050insGGGAA	GRCh37
NC_000006.10:g.88929768_88929769insGGGAA	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369499.3:c.-64+926_-64+927insTTCCC	ENSP00000358511.2:n.-64+926_-64+927insTTC...
ENST00000369501.3:c.-64+2472_-64+2473insTTCCC MANE Select	ENSP00000358513.2:n.-64+2472_-64+2473insT...
ENST00000551417.2:c.-207+926_-207+927insTTCCC	ENSP00000446702.2:n.-207+926_-207+927insT...
ENST00000369499.2:c.-64+926_-64+927insTTCCC	ENSP00000358511.2:n.-64+926_-64+927insTTC...
ENST00000369501.2:c.-64+2472_-64+2473insTTCCC	ENSP00000358513.2:n.-64+2472_-64+2473insT...
ENST00000551417.1:c.-207+926_-207+927insTTCCC	ENSP00000446702.1:n.-207+926_-207+927insT...
NM_001160226.1:c.-207+2472_-207+2473insTTCCC	NP_001153698.1:n.-207+2472_-207+2473insTT...
NM_001160258.1:c.-207+926_-207+927insTTCCC	NP_001153730.1:n.-207+926_-207+927insTTCC...
NM_001160259.1:c.-64+2416_-64+2417insTTCCC	NP_001153731.1:n.-64+2416_-64+2417insTTCC...
NM_016083.4:c.-64+2472_-64+2473insTTCCC	NP_057167.2:n.-64+2472_-64+2473insTTCCC
XM_006715330.2:c.-64+3245_-64+3246insTTCCC	XP_006715393.1:n.-64+3245_-64+3246insTTCC...
XM_011535424.1:c.-255+2472_-255+2473insTTCCC	XP_011533726.1:n.-255+2472_-255+2473insTT...
XM_011535425.1:c.-255+926_-255+927insTTCCC	XP_011533727.1:n.-255+926_-255+927insTTCC...
XM_011535426.1:c.-413+926_-413+927insTTCCC	XP_011533728.1:n.-413+926_-413+927insTTCC...
XM_011535427.1:c.-366+926_-366+927insTTCCC	XP_011533729.1:n.-366+926_-366+927insTTCC...
XM_011535428.1:c.-64+926_-64+927insTTCCC	XP_011533730.1:n.-64+926_-64+927insTTCCC
NM_001160226.2:c.-207+2472_-207+2473insTTCCC	NP_001153698.1:n.-207+2472_-207+2473insTT...
NM_001160258.2:c.-207+926_-207+927insTTCCC	NP_001153730.1:n.-207+926_-207+927insTTCC...
NM_001160259.2:c.-64+2416_-64+2417insTTCCC	NP_001153731.1:n.-64+2416_-64+2417insTTCC...
NM_001365869.1:c.-64+926_-64+927insTTCCC	NP_001352798.1:n.-64+926_-64+927insTTCCC
NM_001365870.1:c.-255+2472_-255+2473insTTCCC	NP_001352799.1:n.-255+2472_-255+2473insTT...
NM_001365872.1:c.-413+926_-413+927insTTCCC	NP_001352801.1:n.-413+926_-413+927insTTCC...
NM_016083.5:c.-64+2472_-64+2473insTTCCC	NP_057167.2:n.-64+2472_-64+2473insTTCCC
XM_006715330.3:c.-64+3245_-64+3246insTTCCC	XP_006715393.1:n.-64+3245_-64+3246insTTCC...
XM_011535425.2:c.-255+926_-255+927insTTCCC	XP_011533727.1:n.-255+926_-255+927insTTCC...
XM_017010240.2:c.-64+3859_-64+3860insTTCCC	XP_016865729.1:n.-64+3859_-64+3860insTTCC...
NM_001160226.3:c.-207+2472_-207+2473insTTCCC	NP_001153698.1:n.-207+2472_-207+2473insTT...
NM_001160258.3:c.-207+926_-207+927insTTCCC	NP_001153730.1:n.-207+926_-207+927insTTCC...
NM_001160259.3:c.-64+2416_-64+2417insTTCCC	NP_001153731.1:n.-64+2416_-64+2417insTTCC...
NM_001365869.2:c.-64+926_-64+927insTTCCC	NP_001352798.1:n.-64+926_-64+927insTTCCC
NM_001365870.2:c.-255+2472_-255+2473insTTCCC	NP_001352799.1:n.-255+2472_-255+2473insTT...
NM_001365872.2:c.-413+926_-413+927insTTCCC	NP_001352801.1:n.-413+926_-413+927insTTCC...
NM_001370545.1:c.-64+3245_-64+3246insTTCCC	NP_001357474.1:n.-64+3245_-64+3246insTTCC...
NM_001370546.1:c.-64+3859_-64+3860insTTCCC	NP_001357475.1:n.-64+3859_-64+3860insTTCC...
NM_001370547.1:c.-255+926_-255+927insTTCCC	NP_001357476.1:n.-255+926_-255+927insTTCC...
NM_016083.6:c.-64+2472_-64+2473insTTCCC MANE Select	NP_057167.2:n.-64+2472_-64+2473insTTCCC