Canonical Allele Identifier: CA2797344985

Gene: CRY1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.107001645_107001646dup , CM000674.2:g.107001645_107001646dup	GRCh38
NC_000012.11:g.107395423_107395424dup , CM000674.1:g.107395423_107395424dup	GRCh37
NC_000012.10:g.105919553_105919554dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000008527.10:c.595+118_595+119dup MANE Select	ENSP00000008527.5:n.595+118_595+119dup
ENST00000008527.9:c.595+118_595+119dup	ENSP00000008527.5:n.595+118_595+119dup
ENST00000546722.1:n.88+118_88+119dup
ENST00000552790.5:n.1154+118_1154+119dup
NM_004075.4:c.595+118_595+119dup	NP_004066.1:n.595+118_595+119dup
XM_011537939.1:c.511+118_511+119dup	XP_011536241.1:n.511+118_511+119dup
XM_017018832.2:c.511+118_511+119dup	XP_016874321.1:n.511+118_511+119dup
XM_024448844.1:c.595+118_595+119dup	XP_024304612.1:n.595+118_595+119dup
XM_024448845.1:c.511+118_511+119dup	XP_024304613.1:n.511+118_511+119dup
NM_004075.5:c.595+118_595+119dup MANE Select	NP_004066.1:n.595+118_595+119dup