Canonical Allele Identifier: CA2797346401
Gene: CRY1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.107058910A>G , CM000674.2:g.107058910A>G GRCh38
NC_000012.11:g.107452688A>G , CM000674.1:g.107452688A>G GRCh37
NC_000012.10:g.105976818A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000008527.10:c.158+33894T>C MANE Select ENSP00000008527.5:n.158+33894T>C
ENST00000008527.9:c.158+33894T>C ENSP00000008527.5:n.158+33894T>C
NM_004075.4:c.158+33894T>C NP_004066.1:n.158+33894T>C
XM_011537939.1:c.74+14025T>C XP_011536241.1:n.74+14025T>C
XM_017018832.2:c.74+14025T>C XP_016874321.1:n.74+14025T>C
XM_024448844.1:c.158+33894T>C XP_024304612.1:n.158+33894T>C
XM_024448845.1:c.74+14025T>C XP_024304613.1:n.74+14025T>C
NM_004075.5:c.158+33894T>C MANE Select NP_004066.1:n.158+33894T>C