Canonical Allele Identifier: CA6764247

Gene: CRY1

Linked Data

• dbSNP Id: rs753176949
• ExAC: 12:107395125 G / T
• gnomAD v2: 12-107395125-G-T
• gnomAD v3: 12-107001347-G-T
• gnomAD v4: 12-107001347-G-T
• MyVariant Identifiers: chr12:g.107395125G>T (hg19) ; chr12:g.107001347G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.107001347G>T , CM000674.2:g.107001347G>T	GRCh38
NC_000012.11:g.107395125G>T , CM000674.1:g.107395125G>T	GRCh37
NC_000012.10:g.105919255G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000008527.10:c.617C>A MANE Select	ENSP00000008527.5:p.Ser206Tyr
ENST00000008527.9:c.617C>A	ENSP00000008527.5:p.Ser206Tyr
ENST00000546722.1:n.110C>A
ENST00000552790.5:n.1176C>A
NM_004075.4:c.617C>A	NP_004066.1:p.Ser206Tyr
XM_011537939.1:c.533C>A	XP_011536241.1:p.Ser178Tyr
XM_017018832.2:c.533C>A	XP_016874321.1:p.Ser178Tyr
XM_024448844.1:c.617C>A	XP_024304612.1:p.Ser206Tyr
XM_024448845.1:c.533C>A	XP_024304613.1:p.Ser178Tyr
NM_004075.5:c.617C>A MANE Select	NP_004066.1:p.Ser206Tyr