Canonical Allele Identifier: CA365061648

Gene: CNR1

Linked Data

• MyVariant Identifiers: chr6:g.88853792C>A (hg19) ; chr6:g.88144073C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.88144073C>A , CM000668.2:g.88144073C>A	GRCh38
NC_000006.11:g.88853792C>A , CM000668.1:g.88853792C>A	GRCh37
NC_000006.10:g.88910511C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362094.6:c.1035G>T	ENSP00000355418.5:n.1035G>T
ENST00000369499.3:c.1202G>T	ENSP00000358511.2:p.Ser401Ile
ENST00000369501.3:c.1202G>T MANE Select	ENSP00000358513.2:p.Ser401Ile
ENST00000428600.3:c.1202G>T	ENSP00000412192.2:p.Ser401Ile
ENST00000468898.2:c.1103G>T	ENSP00000420188.1:p.Ser368Ile
ENST00000549890.2:c.1202G>T	ENSP00000446819.1:p.Ser401Ile
ENST00000551417.2:c.1202G>T	ENSP00000446702.2:p.Ser401Ile
ENST00000362094.5:c.1035G>T	ENSP00000355418.5:n.1035G>T
ENST00000369499.2:c.1202G>T	ENSP00000358511.2:p.Ser401Ile
ENST00000369501.2:c.1202G>T	ENSP00000358513.2:p.Ser401Ile
ENST00000428600.2:c.1202G>T	ENSP00000412192.2:p.Ser401Ile
ENST00000468898.1:c.1103G>T	ENSP00000420188.1:p.Ser368Ile
ENST00000549890.1:c.1202G>T	ENSP00000446819.1:p.Ser401Ile
NM_001160226.1:c.1202G>T	NP_001153698.1:p.Ser401Ile
NM_001160258.1:c.1202G>T	NP_001153730.1:p.Ser401Ile
NM_001160259.1:c.1202G>T	NP_001153731.1:p.Ser401Ile
NM_016083.4:c.1202G>T	NP_057167.2:p.Ser401Ile
NM_033181.3:c.1103G>T	NP_149421.2:p.Ser368Ile
XM_005248650.3:c.1202G>T	XP_005248707.1:p.Ser401Ile
XM_006715330.2:c.1202G>T	XP_006715393.1:p.Ser401Ile
XM_011535424.1:c.1202G>T	XP_011533726.1:p.Ser401Ile
XM_011535425.1:c.1202G>T	XP_011533727.1:p.Ser401Ile
XM_011535426.1:c.1202G>T	XP_011533728.1:p.Ser401Ile
XM_011535427.1:c.1202G>T	XP_011533729.1:p.Ser401Ile
XM_011535428.1:c.1202G>T	XP_011533730.1:p.Ser401Ile
NM_001160226.2:c.1202G>T	NP_001153698.1:p.Ser401Ile
NM_001160258.2:c.1202G>T	NP_001153730.1:p.Ser401Ile
NM_001160259.2:c.1202G>T	NP_001153731.1:p.Ser401Ile
NM_001365869.1:c.1202G>T	NP_001352798.1:p.Ser401Ile
NM_001365870.1:c.1202G>T	NP_001352799.1:p.Ser401Ile
NM_001365872.1:c.1202G>T	NP_001352801.1:p.Ser401Ile
NM_001365874.1:c.1202G>T	NP_001352803.1:p.Ser401Ile
NM_016083.5:c.1202G>T	NP_057167.2:p.Ser401Ile
NM_033181.4:c.1103G>T	NP_149421.2:p.Ser368Ile
XM_006715330.3:c.1202G>T	XP_006715393.1:p.Ser401Ile
XM_011535425.2:c.1202G>T	XP_011533727.1:p.Ser401Ile
XM_017010240.2:c.1202G>T	XP_016865729.1:p.Ser401Ile
NM_001160226.3:c.1202G>T	NP_001153698.1:p.Ser401Ile
NM_001160258.3:c.1202G>T	NP_001153730.1:p.Ser401Ile
NM_001160259.3:c.1202G>T	NP_001153731.1:p.Ser401Ile
NM_001365869.2:c.1202G>T	NP_001352798.1:p.Ser401Ile
NM_001365870.2:c.1202G>T	NP_001352799.1:p.Ser401Ile
NM_001365872.2:c.1202G>T	NP_001352801.1:p.Ser401Ile
NM_001365874.2:c.1202G>T	NP_001352803.1:p.Ser401Ile
NM_001370545.1:c.1202G>T	NP_001357474.1:p.Ser401Ile
NM_001370546.1:c.1202G>T	NP_001357475.1:p.Ser401Ile
NM_001370547.1:c.1202G>T	NP_001357476.1:p.Ser401Ile
NM_016083.6:c.1202G>T MANE Select	NP_057167.2:p.Ser401Ile
NM_001365874.3:c.1202G>T	NP_001352803.1:p.Ser401Ile