Canonical Allele Identifier: CA2061297685

Gene: CRY1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.107001719_107001720delinsAT , CM000674.2:g.107001719_107001720delinsAT	GRCh38
NC_000012.11:g.107395497_107395498delinsAT , CM000674.1:g.107395497_107395498delinsAT	GRCh37
NC_000012.10:g.105919627_105919628delinsAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000008527.10:c.595+44_595+45delinsAT MANE Select	ENSP00000008527.5:n.595+44_595+45delinsAT
ENST00000008527.9:c.595+44_595+45delinsAT	ENSP00000008527.5:n.595+44_595+45delinsAT
ENST00000546722.1:n.88+44_88+45delinsAT
ENST00000552790.5:n.1154+44_1154+45delinsAT
NM_004075.4:c.595+44_595+45delinsAT	NP_004066.1:n.595+44_595+45delinsAT
XM_011537939.1:c.511+44_511+45delinsAT	XP_011536241.1:n.511+44_511+45delinsAT
XM_017018832.2:c.511+44_511+45delinsAT	XP_016874321.1:n.511+44_511+45delinsAT
XM_024448844.1:c.595+44_595+45delinsAT	XP_024304612.1:n.595+44_595+45delinsAT
XM_024448845.1:c.511+44_511+45delinsAT	XP_024304613.1:n.511+44_511+45delinsAT
NM_004075.5:c.595+44_595+45delinsAT MANE Select	NP_004066.1:n.595+44_595+45delinsAT