Canonical Allele Identifier: CA243252031

Gene: CRY1

Linked Data

• dbSNP Id: rs1000662935
• gnomAD v4: 12-107001338-A-G
• MyVariant Identifiers: chr12:g.107395116A>G (hg19) ; chr12:g.107001338A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.107001338A>G , CM000674.2:g.107001338A>G	GRCh38
NC_000012.11:g.107395116A>G , CM000674.1:g.107395116A>G	GRCh37
NC_000012.10:g.105919246A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000008527.10:c.626T>C MANE Select	ENSP00000008527.5:p.Val209Ala
ENST00000008527.9:c.626T>C	ENSP00000008527.5:p.Val209Ala
ENST00000546722.1:n.119T>C
ENST00000552790.5:n.1185T>C
NM_004075.4:c.626T>C	NP_004066.1:p.Val209Ala
XM_011537939.1:c.542T>C	XP_011536241.1:p.Val181Ala
XM_017018832.2:c.542T>C	XP_016874321.1:p.Val181Ala
XM_024448844.1:c.626T>C	XP_024304612.1:p.Val209Ala
XM_024448845.1:c.542T>C	XP_024304613.1:p.Val181Ala
NM_004075.5:c.626T>C MANE Select	NP_004066.1:p.Val209Ala