Canonical Allele Identifier: CA2575276917
Gene: CRY1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.107001230A>G , CM000674.2:g.107001230A>G GRCh38
NC_000012.11:g.107395008A>G , CM000674.1:g.107395008A>G GRCh37
NC_000012.10:g.105919138A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000008527.10:c.684+50T>C MANE Select ENSP00000008527.5:n.684+50T>C
ENST00000008527.9:c.684+50T>C ENSP00000008527.5:n.684+50T>C
ENST00000546722.1:n.177+50T>C
ENST00000552790.5:n.1243+50T>C
NM_004075.4:c.684+50T>C NP_004066.1:n.684+50T>C
XM_011537939.1:c.600+50T>C XP_011536241.1:n.600+50T>C
XM_017018832.2:c.600+50T>C XP_016874321.1:n.600+50T>C
XM_024448844.1:c.684+50T>C XP_024304612.1:n.684+50T>C
XM_024448845.1:c.600+50T>C XP_024304613.1:n.600+50T>C
NM_004075.5:c.684+50T>C MANE Select NP_004066.1:n.684+50T>C
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