Canonical Allele Identifier: CA2061297610

Gene: CRY1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.107001594_107001597delinsAATG , CM000674.2:g.107001594_107001597delinsAATG	GRCh38
NC_000012.11:g.107395372_107395375delinsAATG , CM000674.1:g.107395372_107395375delinsAATG	GRCh37
NC_000012.10:g.105919502_105919505delinsAATG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000008527.10:c.595+167_595+170delinsCATT MANE Select	ENSP00000008527.5:n.595+167_595+170delinsCATT
ENST00000008527.9:c.595+167_595+170delinsCATT	ENSP00000008527.5:n.595+167_595+170delinsCATT
ENST00000546722.1:n.88+167_88+170delinsCATT
ENST00000552790.5:n.1154+167_1154+170delinsCATT
NM_004075.4:c.595+167_595+170delinsCATT	NP_004066.1:n.595+167_595+170delinsCATT
XM_011537939.1:c.511+167_511+170delinsCATT	XP_011536241.1:n.511+167_511+170delinsCATT
XM_017018832.2:c.511+167_511+170delinsCATT	XP_016874321.1:n.511+167_511+170delinsCATT
XM_024448844.1:c.595+167_595+170delinsCATT	XP_024304612.1:n.595+167_595+170delinsCATT
XM_024448845.1:c.511+167_511+170delinsCATT	XP_024304613.1:n.511+167_511+170delinsCATT
NM_004075.5:c.595+167_595+170delinsCATT MANE Select	NP_004066.1:n.595+167_595+170delinsCATT