Canonical Allele Identifier: CA2061297255

Gene: CRY1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.107001191_107001195delinsCTATT , CM000674.2:g.107001191_107001195delinsCTATT	GRCh38
NC_000012.11:g.107394969_107394973delinsCTATT , CM000674.1:g.107394969_107394973delinsCTATT	GRCh37
NC_000012.10:g.105919099_105919103delinsCTATT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000008527.10:c.684+85_684+89delinsAATAG MANE Select	ENSP00000008527.5:n.684+85_684+89delinsAATAG
ENST00000008527.9:c.684+85_684+89delinsAATAG	ENSP00000008527.5:n.684+85_684+89delinsAATAG
ENST00000546722.1:n.177+85_177+89delinsAATAG
ENST00000552790.5:n.1243+85_1243+89delinsAATAG
NM_004075.4:c.684+85_684+89delinsAATAG	NP_004066.1:n.684+85_684+89delinsAATAG
XM_011537939.1:c.600+85_600+89delinsAATAG	XP_011536241.1:n.600+85_600+89delinsAATAG
XM_017018832.2:c.600+85_600+89delinsAATAG	XP_016874321.1:n.600+85_600+89delinsAATAG
XM_024448844.1:c.684+85_684+89delinsAATAG	XP_024304612.1:n.684+85_684+89delinsAATAG
XM_024448845.1:c.600+85_600+89delinsAATAG	XP_024304613.1:n.600+85_600+89delinsAATAG
NM_004075.5:c.684+85_684+89delinsAATAG MANE Select	NP_004066.1:n.684+85_684+89delinsAATAG