Canonical Allele Identifier: CA386405128

Gene: CRY1

Linked Data

• dbSNP Id: rs1415167088
• gnomAD v2: 12-107395141-C-A
• gnomAD v4: 12-107001363-C-A
• MyVariant Identifiers: chr12:g.107395141C>A (hg19) ; chr12:g.107001363C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.107001363C>A , CM000674.2:g.107001363C>A	GRCh38
NC_000012.11:g.107395141C>A , CM000674.1:g.107395141C>A	GRCh37
NC_000012.10:g.105919271C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000008527.10:c.601G>T MANE Select	ENSP00000008527.5:p.Asp201Tyr
ENST00000008527.9:c.601G>T	ENSP00000008527.5:p.Asp201Tyr
ENST00000546722.1:n.94G>T
ENST00000552790.5:n.1160G>T
NM_004075.4:c.601G>T	NP_004066.1:p.Asp201Tyr
XM_011537939.1:c.517G>T	XP_011536241.1:p.Asp173Tyr
XM_017018832.2:c.517G>T	XP_016874321.1:p.Asp173Tyr
XM_024448844.1:c.601G>T	XP_024304612.1:p.Asp201Tyr
XM_024448845.1:c.517G>T	XP_024304613.1:p.Asp173Tyr
NM_004075.5:c.601G>T MANE Select	NP_004066.1:p.Asp201Tyr