Canonical Allele Identifier: CA607600072

Gene: CRY1

Linked Data

• dbSNP Id: rs1426496308
• gnomAD v2: 12-107395526-T-G
• gnomAD v4: 12-107001748-T-G
• MyVariant Identifiers: chr12:g.107395526T>G (hg19) ; chr12:g.107001748T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.107001748T>G , CM000674.2:g.107001748T>G	GRCh38
NC_000012.11:g.107395526T>G , CM000674.1:g.107395526T>G	GRCh37
NC_000012.10:g.105919656T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000008527.10:c.595+16A>C MANE Select	ENSP00000008527.5:n.595+16A>C
ENST00000008527.9:c.595+16A>C	ENSP00000008527.5:n.595+16A>C
ENST00000546722.1:n.88+16A>C
ENST00000552790.5:n.1154+16A>C
NM_004075.4:c.595+16A>C	NP_004066.1:n.595+16A>C
XM_011537939.1:c.511+16A>C	XP_011536241.1:n.511+16A>C
XM_017018832.2:c.511+16A>C	XP_016874321.1:n.511+16A>C
XM_024448844.1:c.595+16A>C	XP_024304612.1:n.595+16A>C
XM_024448845.1:c.511+16A>C	XP_024304613.1:n.511+16A>C
NM_004075.5:c.595+16A>C MANE Select	NP_004066.1:n.595+16A>C