Canonical Allele Identifier: CA6764242
Gene: CRY1 HGNC NCBI

Linked Data

dbSNP Id: rs8192440

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.107001328A>G , CM000674.2:g.107001328A>G GRCh38
NC_000012.11:g.107395106A>G , CM000674.1:g.107395106A>G GRCh37
NC_000012.10:g.105919236A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000008527.10:c.636T>C MANE Select ENSP00000008527.5:p.Gly212=
ENST00000008527.9:c.636T>C ENSP00000008527.5:p.Gly212=
ENST00000546722.1:n.129T>C
ENST00000552790.5:n.1195T>C
NM_004075.4:c.636T>C NP_004066.1:p.Gly212=
XM_011537939.1:c.552T>C XP_011536241.1:p.Gly184=
XM_017018832.2:c.552T>C XP_016874321.1:p.Gly184=
XM_024448844.1:c.636T>C XP_024304612.1:p.Gly212=
XM_024448845.1:c.552T>C XP_024304613.1:p.Gly184=
NM_004075.5:c.636T>C MANE Select NP_004066.1:p.Gly212=