Canonical Allele Identifier: CA951511479

Gene: CRY1

Linked Data

• dbSNP Id: rs1952305028
• gnomAD v3: 12-107001198-T-C
• gnomAD v4: 12-107001198-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.107001198T>C , CM000674.2:g.107001198T>C	GRCh38
NC_000012.11:g.107394976T>C , CM000674.1:g.107394976T>C	GRCh37
NC_000012.10:g.105919106T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000008527.10:c.684+82A>G MANE Select	ENSP00000008527.5:n.684+82A>G
ENST00000008527.9:c.684+82A>G	ENSP00000008527.5:n.684+82A>G
ENST00000546722.1:n.177+82A>G
ENST00000552790.5:n.1243+82A>G
NM_004075.4:c.684+82A>G	NP_004066.1:n.684+82A>G
XM_011537939.1:c.600+82A>G	XP_011536241.1:n.600+82A>G
XM_017018832.2:c.600+82A>G	XP_016874321.1:n.600+82A>G
XM_024448844.1:c.684+82A>G	XP_024304612.1:n.684+82A>G
XM_024448845.1:c.600+82A>G	XP_024304613.1:n.600+82A>G
NM_004075.5:c.684+82A>G MANE Select	NP_004066.1:n.684+82A>G