Canonical Allele Identifier: CA2620676923
Gene: CRY1 HGNC NCBI

Linked Data

gnomAD v4: 12-107001719-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.107001719A>T , CM000674.2:g.107001719A>T GRCh38
NC_000012.11:g.107395497A>T , CM000674.1:g.107395497A>T GRCh37
NC_000012.10:g.105919627A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000008527.10:c.595+45T>A MANE Select ENSP00000008527.5:n.595+45T>A
ENST00000008527.9:c.595+45T>A ENSP00000008527.5:n.595+45T>A
ENST00000546722.1:n.88+45T>A
ENST00000552790.5:n.1154+45T>A
NM_004075.4:c.595+45T>A NP_004066.1:n.595+45T>A
XM_011537939.1:c.511+45T>A XP_011536241.1:n.511+45T>A
XM_017018832.2:c.511+45T>A XP_016874321.1:n.511+45T>A
XM_024448844.1:c.595+45T>A XP_024304612.1:n.595+45T>A
XM_024448845.1:c.511+45T>A XP_024304613.1:n.511+45T>A
NM_004075.5:c.595+45T>A MANE Select NP_004066.1:n.595+45T>A
Search 100 bp 5'
Search 100 bp 3'