Canonical Allele Identifier: CA2620676695

Gene: CRY1

Linked Data

• gnomAD v4: 12-107001219-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.107001219_107001220insC , CM000674.2:g.107001219_107001220insC	GRCh38
NC_000012.11:g.107394997_107394998insC , CM000674.1:g.107394997_107394998insC	GRCh37
NC_000012.10:g.105919127_105919128insC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000008527.10:c.684+60_684+61insG MANE Select	ENSP00000008527.5:n.684+60_684+61insG
ENST00000008527.9:c.684+60_684+61insG	ENSP00000008527.5:n.684+60_684+61insG
ENST00000546722.1:n.177+60_177+61insG
ENST00000552790.5:n.1243+60_1243+61insG
NM_004075.4:c.684+60_684+61insG	NP_004066.1:n.684+60_684+61insG
XM_011537939.1:c.600+60_600+61insG	XP_011536241.1:n.600+60_600+61insG
XM_017018832.2:c.600+60_600+61insG	XP_016874321.1:n.600+60_600+61insG
XM_024448844.1:c.684+60_684+61insG	XP_024304612.1:n.684+60_684+61insG
XM_024448845.1:c.600+60_600+61insG	XP_024304613.1:n.600+60_600+61insG
NM_004075.5:c.684+60_684+61insG MANE Select	NP_004066.1:n.684+60_684+61insG