Canonical Allele Identifier: CA386405105

Gene: CRY1

Linked Data

• dbSNP Id: rs1952308962
• MyVariant Identifiers: chr12:g.107395137G>T (hg19) ; chr12:g.107001359G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.107001359G>T , CM000674.2:g.107001359G>T	GRCh38
NC_000012.11:g.107395137G>T , CM000674.1:g.107395137G>T	GRCh37
NC_000012.10:g.105919267G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000008527.10:c.605C>A MANE Select	ENSP00000008527.5:p.Thr202Lys
ENST00000008527.9:c.605C>A	ENSP00000008527.5:p.Thr202Lys
ENST00000546722.1:n.98C>A
ENST00000552790.5:n.1164C>A
NM_004075.4:c.605C>A	NP_004066.1:p.Thr202Lys
XM_011537939.1:c.521C>A	XP_011536241.1:p.Thr174Lys
XM_017018832.2:c.521C>A	XP_016874321.1:p.Thr174Lys
XM_024448844.1:c.605C>A	XP_024304612.1:p.Thr202Lys
XM_024448845.1:c.521C>A	XP_024304613.1:p.Thr174Lys
NM_004075.5:c.605C>A MANE Select	NP_004066.1:p.Thr202Lys