Canonical Allele Identifier: CA2620676673

Gene: CRY1

Linked Data

• gnomAD v4: 12-107001173-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.107001173_107001174insA , CM000674.2:g.107001173_107001174insA	GRCh38
NC_000012.11:g.107394951_107394952insA , CM000674.1:g.107394951_107394952insA	GRCh37
NC_000012.10:g.105919081_105919082insA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000008527.10:c.684+106_684+107insT MANE Select	ENSP00000008527.5:n.684+106_684+107insT
ENST00000008527.9:c.684+106_684+107insT	ENSP00000008527.5:n.684+106_684+107insT
ENST00000546722.1:n.177+106_177+107insT
ENST00000552790.5:n.1243+106_1243+107insT
NM_004075.4:c.684+106_684+107insT	NP_004066.1:n.684+106_684+107insT
XM_011537939.1:c.600+106_600+107insT	XP_011536241.1:n.600+106_600+107insT
XM_017018832.2:c.600+106_600+107insT	XP_016874321.1:n.600+106_600+107insT
XM_024448844.1:c.684+106_684+107insT	XP_024304612.1:n.684+106_684+107insT
XM_024448845.1:c.600+106_600+107insT	XP_024304613.1:n.600+106_600+107insT
NM_004075.5:c.684+106_684+107insT MANE Select	NP_004066.1:n.684+106_684+107insT