Canonical Allele Identifier: CA2061297592

Gene: CRY1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.107001549C= , CM000674.2:g.107001549C=	GRCh38
NC_000012.11:g.107395327C= , CM000674.1:g.107395327C=	GRCh37
NC_000012.10:g.105919457C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000008527.10:c.596-181G= MANE Select	ENSP00000008527.5:n.596-181G=
ENST00000008527.9:c.596-181G=	ENSP00000008527.5:n.596-181G=
ENST00000546722.1:n.89-181G=
ENST00000552790.5:n.1155-181G=
NM_004075.4:c.596-181G=	NP_004066.1:n.596-181G=
XM_011537939.1:c.512-181G=	XP_011536241.1:n.512-181G=
XM_017018832.2:c.512-181G=	XP_016874321.1:n.512-181G=
XM_024448844.1:c.596-181G=	XP_024304612.1:n.596-181G=
XM_024448845.1:c.512-181G=	XP_024304613.1:n.512-181G=
NM_004075.5:c.596-181G= MANE Select	NP_004066.1:n.596-181G=