Canonical Allele Identifier: CA2061322699

Gene: CRY1

Linked Data

• dbSNP Id: rs1953018011

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.107059032_107059034del , CM000674.2:g.107059032_107059034del	GRCh38
NC_000012.11:g.107452810_107452812del , CM000674.1:g.107452810_107452812del	GRCh37
NC_000012.10:g.105976940_105976942del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000008527.10:c.158+33770_158+33772del MANE Select	ENSP00000008527.5:n.158+33770_158+33772de...
ENST00000008527.9:c.158+33770_158+33772del	ENSP00000008527.5:n.158+33770_158+33772de...
NM_004075.4:c.158+33770_158+33772del	NP_004066.1:n.158+33770_158+33772del
XM_011537939.1:c.74+13901_74+13903del	XP_011536241.1:n.74+13901_74+13903del
XM_017018832.2:c.74+13901_74+13903del	XP_016874321.1:n.74+13901_74+13903del
XM_024448844.1:c.158+33770_158+33772del	XP_024304612.1:n.158+33770_158+33772del
XM_024448845.1:c.74+13901_74+13903del	XP_024304613.1:n.74+13901_74+13903del
NM_004075.5:c.158+33770_158+33772del MANE Select	NP_004066.1:n.158+33770_158+33772del