Canonical Allele Identifier: CA6764241

Gene: CRY1

Linked Data

• dbSNP Id: rs776553940
• ExAC: 12:107395105 C / T
• gnomAD v2: 12-107395105-C-T
• gnomAD v3: 12-107001327-C-T
• gnomAD v4: 12-107001327-C-T
• MyVariant Identifiers: chr12:g.107395105C>T (hg19) ; chr12:g.107001327C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.107001327C>T , CM000674.2:g.107001327C>T	GRCh38
NC_000012.11:g.107395105C>T , CM000674.1:g.107395105C>T	GRCh37
NC_000012.10:g.105919235C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000008527.10:c.637G>A MANE Select	ENSP00000008527.5:p.Gly213Arg
ENST00000008527.9:c.637G>A	ENSP00000008527.5:p.Gly213Arg
ENST00000546722.1:n.130G>A
ENST00000552790.5:n.1196G>A
NM_004075.4:c.637G>A	NP_004066.1:p.Gly213Arg
XM_011537939.1:c.553G>A	XP_011536241.1:p.Gly185Arg
XM_017018832.2:c.553G>A	XP_016874321.1:p.Gly185Arg
XM_024448844.1:c.637G>A	XP_024304612.1:p.Gly213Arg
XM_024448845.1:c.553G>A	XP_024304613.1:p.Gly185Arg
NM_004075.5:c.637G>A MANE Select	NP_004066.1:p.Gly213Arg