Canonical Allele Identifier: CA386404594
Gene: CRY1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.107001290A>C , CM000674.2:g.107001290A>C GRCh38
NC_000012.11:g.107395068A>C , CM000674.1:g.107395068A>C GRCh37
NC_000012.10:g.105919198A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000008527.10:c.674T>G MANE Select ENSP00000008527.5:p.Leu225Trp
ENST00000008527.9:c.674T>G ENSP00000008527.5:p.Leu225Trp
ENST00000546722.1:n.167T>G
ENST00000552790.5:n.1233T>G
NM_004075.4:c.674T>G NP_004066.1:p.Leu225Trp
XM_011537939.1:c.590T>G XP_011536241.1:p.Leu197Trp
XM_017018832.2:c.590T>G XP_016874321.1:p.Leu197Trp
XM_024448844.1:c.674T>G XP_024304612.1:p.Leu225Trp
XM_024448845.1:c.590T>G XP_024304613.1:p.Leu197Trp
NM_004075.5:c.674T>G MANE Select NP_004066.1:p.Leu225Trp