Canonical Allele Identifier: CA2061297680

Gene: CRY1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.107001718_107001722delinsGATTT , CM000674.2:g.107001718_107001722delinsGATTT	GRCh38
NC_000012.11:g.107395496_107395500delinsGATTT , CM000674.1:g.107395496_107395500delinsGATTT	GRCh37
NC_000012.10:g.105919626_105919630delinsGATTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000008527.10:c.595+42_595+46delinsAAATC MANE Select	ENSP00000008527.5:n.595+42_595+46delinsAAATC
ENST00000008527.9:c.595+42_595+46delinsAAATC	ENSP00000008527.5:n.595+42_595+46delinsAAATC
ENST00000546722.1:n.88+42_88+46delinsAAATC
ENST00000552790.5:n.1154+42_1154+46delinsAAATC
NM_004075.4:c.595+42_595+46delinsAAATC	NP_004066.1:n.595+42_595+46delinsAAATC
XM_011537939.1:c.511+42_511+46delinsAAATC	XP_011536241.1:n.511+42_511+46delinsAAATC
XM_017018832.2:c.511+42_511+46delinsAAATC	XP_016874321.1:n.511+42_511+46delinsAAATC
XM_024448844.1:c.595+42_595+46delinsAAATC	XP_024304612.1:n.595+42_595+46delinsAAATC
XM_024448845.1:c.511+42_511+46delinsAAATC	XP_024304613.1:n.511+42_511+46delinsAAATC
NM_004075.5:c.595+42_595+46delinsAAATC MANE Select	NP_004066.1:n.595+42_595+46delinsAAATC