Canonical Allele Identifier: CA2061297401

Gene: CRY1

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000008527.10:c.637G= MANE Select	ENSP00000008527.5:p.Gly213=
ENST00000008527.9:c.637G=	ENSP00000008527.5:p.Gly213=
ENST00000546722.1:n.130G=
ENST00000552790.5:n.1196G=
NM_004075.4:c.637G=	NP_004066.1:p.Gly213=
XM_011537939.1:c.553G=	XP_011536241.1:p.Gly185=
XM_017018832.2:c.553G=	XP_016874321.1:p.Gly185=
XM_024448844.1:c.637G=	XP_024304612.1:p.Gly213=
XM_024448845.1:c.553G=	XP_024304613.1:p.Gly185=
NM_004075.5:c.637G= MANE Select	NP_004066.1:p.Gly213=