Canonical Allele Identifier: CA2061293130

Gene: CRY1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.106992962T= , CM000674.2:g.106992962T=	GRCh38
NC_000012.11:g.107386740T= , CM000674.1:g.107386740T=	GRCh37
NC_000012.10:g.105910870T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_004075.5:c.1657+3A= MANE Select	NP_004066.1:n.1657+3A=
ENST00000008527.10:c.1657+3A= MANE Select	ENSP00000008527.5:n.1657+3A=
NM_004075.4:c.1657+3A=	NP_004066.1:n.1657+3A=
ENST00000008527.9:c.1657+3A=	ENSP00000008527.5:n.1657+3A=
ENST00000549356.1:c.217+3A=	ENSP00000447738.1:n.217+3A=
ENST00000552790.5:n.2239A=
XM_011537939.1:c.1573+3A=	XP_011536241.1:n.1573+3A=
XM_017018832.2:c.1573+3A=	XP_016874321.1:n.1573+3A=
XM_024448844.1:c.1660A=	XP_024304612.1:p.Lys554=
XM_024448845.1:c.1576A=	XP_024304613.1:p.Lys526=