Canonical Allele Identifier: CA386404738
Gene: CRY1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.107001305C>G , CM000674.2:g.107001305C>G GRCh38
NC_000012.11:g.107395083C>G , CM000674.1:g.107395083C>G GRCh37
NC_000012.10:g.105919213C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000008527.10:c.659G>C MANE Select ENSP00000008527.5:p.Arg220Pro
ENST00000008527.9:c.659G>C ENSP00000008527.5:p.Arg220Pro
ENST00000546722.1:n.152G>C
ENST00000552790.5:n.1218G>C
NM_004075.4:c.659G>C NP_004066.1:p.Arg220Pro
XM_011537939.1:c.575G>C XP_011536241.1:p.Arg192Pro
XM_017018832.2:c.575G>C XP_016874321.1:p.Arg192Pro
XM_024448844.1:c.659G>C XP_024304612.1:p.Arg220Pro
XM_024448845.1:c.575G>C XP_024304613.1:p.Arg192Pro
NM_004075.5:c.659G>C MANE Select NP_004066.1:p.Arg220Pro