Canonical Allele Identifier: CA2061297664

Gene: CRY1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.107001688_107001689delinsAT , CM000674.2:g.107001688_107001689delinsAT	GRCh38
NC_000012.11:g.107395466_107395467delinsAT , CM000674.1:g.107395466_107395467delinsAT	GRCh37
NC_000012.10:g.105919596_105919597delinsAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000008527.10:c.595+75_595+76delinsAT MANE Select	ENSP00000008527.5:n.595+75_595+76delinsAT
ENST00000008527.9:c.595+75_595+76delinsAT	ENSP00000008527.5:n.595+75_595+76delinsAT
ENST00000546722.1:n.88+75_88+76delinsAT
ENST00000552790.5:n.1154+75_1154+76delinsAT
NM_004075.4:c.595+75_595+76delinsAT	NP_004066.1:n.595+75_595+76delinsAT
XM_011537939.1:c.511+75_511+76delinsAT	XP_011536241.1:n.511+75_511+76delinsAT
XM_017018832.2:c.511+75_511+76delinsAT	XP_016874321.1:n.511+75_511+76delinsAT
XM_024448844.1:c.595+75_595+76delinsAT	XP_024304612.1:n.595+75_595+76delinsAT
XM_024448845.1:c.511+75_511+76delinsAT	XP_024304613.1:n.511+75_511+76delinsAT
NM_004075.5:c.595+75_595+76delinsAT MANE Select	NP_004066.1:n.595+75_595+76delinsAT