Canonical Allele Identifier: CA2727014033

Gene: CRY1

Linked Data

• dbSNP Id: rs2136823284

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.107001371_107001372insGCTCTT , CM000674.2:g.107001371_107001372insGCTCTT	GRCh38
NC_000012.11:g.107395149_107395150insGCTCTT , CM000674.1:g.107395149_107395150insGCTCTT	GRCh37
NC_000012.10:g.105919279_105919280insGCTCTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000008527.10:c.596-4_596-3insAAGAGC MANE Select	ENSP00000008527.5:n.596-4_596-3insAAGAGC
ENST00000008527.9:c.596-4_596-3insAAGAGC	ENSP00000008527.5:n.596-4_596-3insAAGAGC
ENST00000546722.1:n.89-4_89-3insAAGAGC
ENST00000552790.5:n.1155-4_1155-3insAAGAGC
NM_004075.4:c.596-4_596-3insAAGAGC	NP_004066.1:n.596-4_596-3insAAGAGC
XM_011537939.1:c.512-4_512-3insAAGAGC	XP_011536241.1:n.512-4_512-3insAAGAGC
XM_017018832.2:c.512-4_512-3insAAGAGC	XP_016874321.1:n.512-4_512-3insAAGAGC
XM_024448844.1:c.596-4_596-3insAAGAGC	XP_024304612.1:n.596-4_596-3insAAGAGC
XM_024448845.1:c.512-4_512-3insAAGAGC	XP_024304613.1:n.512-4_512-3insAAGAGC
NM_004075.5:c.596-4_596-3insAAGAGC MANE Select	NP_004066.1:n.596-4_596-3insAAGAGC