Canonical Allele Identifier: CA2061297410
Gene: CRY1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.107001329C= , CM000674.2:g.107001329C= GRCh38
NC_000012.11:g.107395107C= , CM000674.1:g.107395107C= GRCh37
NC_000012.10:g.105919237C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000008527.10:c.635G= MANE Select ENSP00000008527.5:p.Gly212=
ENST00000008527.9:c.635G= ENSP00000008527.5:p.Gly212=
ENST00000546722.1:n.128G=
ENST00000552790.5:n.1194G=
NM_004075.4:c.635G= NP_004066.1:p.Gly212=
XM_011537939.1:c.551G= XP_011536241.1:p.Gly184=
XM_017018832.2:c.551G= XP_016874321.1:p.Gly184=
XM_024448844.1:c.635G= XP_024304612.1:p.Gly212=
XM_024448845.1:c.551G= XP_024304613.1:p.Gly184=
NM_004075.5:c.635G= MANE Select NP_004066.1:p.Gly212=