Canonical Allele Identifier: CA2620676661
Gene: CRY1 HGNC NCBI

Linked Data

gnomAD v4: 12-107001150-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.107001150G>T , CM000674.2:g.107001150G>T GRCh38
NC_000012.11:g.107394928G>T , CM000674.1:g.107394928G>T GRCh37
NC_000012.10:g.105919058G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000008527.10:c.684+130C>A MANE Select ENSP00000008527.5:n.684+130C>A
ENST00000008527.9:c.684+130C>A ENSP00000008527.5:n.684+130C>A
ENST00000546722.1:n.177+130C>A
ENST00000552790.5:n.1243+130C>A
NM_004075.4:c.684+130C>A NP_004066.1:n.684+130C>A
XM_011537939.1:c.600+130C>A XP_011536241.1:n.600+130C>A
XM_017018832.2:c.600+130C>A XP_016874321.1:n.600+130C>A
XM_024448844.1:c.684+130C>A XP_024304612.1:n.684+130C>A
XM_024448845.1:c.600+130C>A XP_024304613.1:n.600+130C>A
NM_004075.5:c.684+130C>A MANE Select NP_004066.1:n.684+130C>A
Search 100 bp 5'
Search 100 bp 3'