Canonical Allele Identifier: CA607242555
Gene: CRY1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.107395163del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.107001391del , CM000674.2:g.107001391del GRCh38
NC_000012.11:g.107395169del , CM000674.1:g.107395169del GRCh37
NC_000012.10:g.105919299del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000008527.10:c.596-17del MANE Select ENSP00000008527.5:n.596-17del
ENST00000008527.9:c.596-17del ENSP00000008527.5:n.596-17del
ENST00000546722.1:n.89-17del
ENST00000552790.5:n.1155-17del
NM_004075.4:c.596-17del NP_004066.1:n.596-17del
XM_011537939.1:c.512-17del XP_011536241.1:n.512-17del
XM_017018832.2:c.512-17del XP_016874321.1:n.512-17del
XM_024448844.1:c.596-17del XP_024304612.1:n.596-17del
XM_024448845.1:c.512-17del XP_024304613.1:n.512-17del
NM_004075.5:c.596-17del MANE Select NP_004066.1:n.596-17del