Canonical Allele Identifier: CA2061297233

Gene: CRY1

Linked Data

• dbSNP Id: rs1952304491
• gnomAD v4: 12-107001158-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.107001158A>G , CM000674.2:g.107001158A>G	GRCh38
NC_000012.11:g.107394936A>G , CM000674.1:g.107394936A>G	GRCh37
NC_000012.10:g.105919066A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000008527.10:c.684+122T>C MANE Select	ENSP00000008527.5:n.684+122T>C
ENST00000008527.9:c.684+122T>C	ENSP00000008527.5:n.684+122T>C
ENST00000546722.1:n.177+122T>C
ENST00000552790.5:n.1243+122T>C
NM_004075.4:c.684+122T>C	NP_004066.1:n.684+122T>C
XM_011537939.1:c.600+122T>C	XP_011536241.1:n.600+122T>C
XM_017018832.2:c.600+122T>C	XP_016874321.1:n.600+122T>C
XM_024448844.1:c.684+122T>C	XP_024304612.1:n.684+122T>C
XM_024448845.1:c.600+122T>C	XP_024304613.1:n.600+122T>C
NM_004075.5:c.684+122T>C MANE Select	NP_004066.1:n.684+122T>C