Canonical Allele Identifier: CA2575276938
Gene: CRY1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.107001698dup , CM000674.2:g.107001698dup GRCh38
NC_000012.11:g.107395476dup , CM000674.1:g.107395476dup GRCh37
NC_000012.10:g.105919606dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000008527.10:c.595+69dup MANE Select ENSP00000008527.5:n.595+69dup
ENST00000008527.9:c.595+69dup ENSP00000008527.5:n.595+69dup
ENST00000546722.1:n.88+69dup
ENST00000552790.5:n.1154+69dup
NM_004075.4:c.595+69dup NP_004066.1:n.595+69dup
XM_011537939.1:c.511+69dup XP_011536241.1:n.511+69dup
XM_017018832.2:c.511+69dup XP_016874321.1:n.511+69dup
XM_024448844.1:c.595+69dup XP_024304612.1:n.595+69dup
XM_024448845.1:c.511+69dup XP_024304613.1:n.511+69dup
NM_004075.5:c.595+69dup MANE Select NP_004066.1:n.595+69dup