Canonical Allele Identifier: CA6764250
Gene: CRY1 HGNC NCBI

Linked Data

dbSNP Id: rs754173809

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.107001357C>T , CM000674.2:g.107001357C>T GRCh38
NC_000012.11:g.107395135C>T , CM000674.1:g.107395135C>T GRCh37
NC_000012.10:g.105919265C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000008527.10:c.607G>A MANE Select ENSP00000008527.5:p.Asp203Asn
ENST00000008527.9:c.607G>A ENSP00000008527.5:p.Asp203Asn
ENST00000546722.1:n.100G>A
ENST00000552790.5:n.1166G>A
NM_004075.4:c.607G>A NP_004066.1:p.Asp203Asn
XM_011537939.1:c.523G>A XP_011536241.1:p.Asp175Asn
XM_017018832.2:c.523G>A XP_016874321.1:p.Asp175Asn
XM_024448844.1:c.607G>A XP_024304612.1:p.Asp203Asn
XM_024448845.1:c.523G>A XP_024304613.1:p.Asp175Asn
NM_004075.5:c.607G>A MANE Select NP_004066.1:p.Asp203Asn