Canonical Allele Identifier: CA2061297753

Gene: CRY1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.107001783G= , CM000674.2:g.107001783G=	GRCh38
NC_000012.11:g.107395561G= , CM000674.1:g.107395561G=	GRCh37
NC_000012.10:g.105919691G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000008527.10:c.576C= MANE Select	ENSP00000008527.5:p.Val192=
ENST00000008527.9:c.576C=	ENSP00000008527.5:p.Val192=
ENST00000546722.1:n.69C=
ENST00000552790.5:n.1135C=
NM_004075.4:c.576C=	NP_004066.1:p.Val192=
XM_011537939.1:c.492C=	XP_011536241.1:p.Val164=
XM_017018832.2:c.492C=	XP_016874321.1:p.Val164=
XM_024448844.1:c.576C=	XP_024304612.1:p.Val192=
XM_024448845.1:c.492C=	XP_024304613.1:p.Val164=
NM_004075.5:c.576C= MANE Select	NP_004066.1:p.Val192=