Canonical Allele Identifier: CA386405012
Gene: CRY1 HGNC NCBI

Linked Data

dbSNP Id: rs1207204981

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.107001339C>T , CM000674.2:g.107001339C>T GRCh38
NC_000012.11:g.107395117C>T , CM000674.1:g.107395117C>T GRCh37
NC_000012.10:g.105919247C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000008527.10:c.625G>A MANE Select ENSP00000008527.5:p.Val209Met
ENST00000008527.9:c.625G>A ENSP00000008527.5:p.Val209Met
ENST00000546722.1:n.118G>A
ENST00000552790.5:n.1184G>A
NM_004075.4:c.625G>A NP_004066.1:p.Val209Met
XM_011537939.1:c.541G>A XP_011536241.1:p.Val181Met
XM_017018832.2:c.541G>A XP_016874321.1:p.Val181Met
XM_024448844.1:c.625G>A XP_024304612.1:p.Val209Met
XM_024448845.1:c.541G>A XP_024304613.1:p.Val181Met
NM_004075.5:c.625G>A MANE Select NP_004066.1:p.Val209Met