Canonical Allele Identifier: CA481656634

Gene: CRY1

Linked Data

• dbSNP Id: rs1952306999
• MyVariant Identifiers: chr12:g.107395079C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.107001301C>T , CM000674.2:g.107001301C>T	GRCh38
NC_000012.11:g.107395079C>T , CM000674.1:g.107395079C>T	GRCh37
NC_000012.10:g.105919209C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000008527.10:c.663G>A MANE Select	ENSP00000008527.5:p.Leu221=
ENST00000008527.9:c.663G>A	ENSP00000008527.5:p.Leu221=
ENST00000546722.1:n.156G>A
ENST00000552790.5:n.1222G>A
NM_004075.4:c.663G>A	NP_004066.1:p.Leu221=
XM_011537939.1:c.579G>A	XP_011536241.1:p.Leu193=
XM_017018832.2:c.579G>A	XP_016874321.1:p.Leu193=
XM_024448844.1:c.663G>A	XP_024304612.1:p.Leu221=
XM_024448845.1:c.579G>A	XP_024304613.1:p.Leu193=
NM_004075.5:c.663G>A MANE Select	NP_004066.1:p.Leu221=