Canonical Allele Identifier: CA951511494
Gene: CRY1 HGNC NCBI

Linked Data

dbSNP Id: rs1952305970
gnomAD v3: 12-107001248-C-G
gnomAD v4: 12-107001248-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.107001248C>G , CM000674.2:g.107001248C>G GRCh38
NC_000012.11:g.107395026C>G , CM000674.1:g.107395026C>G GRCh37
NC_000012.10:g.105919156C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000008527.10:c.684+32G>C MANE Select ENSP00000008527.5:n.684+32G>C
ENST00000008527.9:c.684+32G>C ENSP00000008527.5:n.684+32G>C
ENST00000546722.1:n.177+32G>C
ENST00000552790.5:n.1243+32G>C
NM_004075.4:c.684+32G>C NP_004066.1:n.684+32G>C
XM_011537939.1:c.600+32G>C XP_011536241.1:n.600+32G>C
XM_017018832.2:c.600+32G>C XP_016874321.1:n.600+32G>C
XM_024448844.1:c.684+32G>C XP_024304612.1:n.684+32G>C
XM_024448845.1:c.600+32G>C XP_024304613.1:n.600+32G>C
NM_004075.5:c.684+32G>C MANE Select NP_004066.1:n.684+32G>C
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