Canonical Allele Identifier: CA2531255619

Gene: CRY1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.107001496_107001497insGCT , CM000674.2:g.107001496_107001497insGCT	GRCh38
NC_000012.11:g.107395274_107395275insGCT , CM000674.1:g.107395274_107395275insGCT	GRCh37
NC_000012.10:g.105919404_105919405insGCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000008527.10:c.596-129_596-128insAGC MANE Select	ENSP00000008527.5:n.596-129_596-128insAGC
ENST00000008527.9:c.596-129_596-128insAGC	ENSP00000008527.5:n.596-129_596-128insAGC
ENST00000546722.1:n.89-129_89-128insAGC
ENST00000552790.5:n.1155-129_1155-128insAGC
NM_004075.4:c.596-129_596-128insAGC	NP_004066.1:n.596-129_596-128insAGC
XM_011537939.1:c.512-129_512-128insAGC	XP_011536241.1:n.512-129_512-128insAGC
XM_017018832.2:c.512-129_512-128insAGC	XP_016874321.1:n.512-129_512-128insAGC
XM_024448844.1:c.596-129_596-128insAGC	XP_024304612.1:n.596-129_596-128insAGC
XM_024448845.1:c.512-129_512-128insAGC	XP_024304613.1:n.512-129_512-128insAGC
NM_004075.5:c.596-129_596-128insAGC MANE Select	NP_004066.1:n.596-129_596-128insAGC