Canonical Allele Identifier: CA2575276916

Gene: CRY1

Linked Data

• gnomAD v4: 12-107001229-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.107001229A>T , CM000674.2:g.107001229A>T	GRCh38
NC_000012.11:g.107395007A>T , CM000674.1:g.107395007A>T	GRCh37
NC_000012.10:g.105919137A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000008527.10:c.684+51T>A MANE Select	ENSP00000008527.5:n.684+51T>A
ENST00000008527.9:c.684+51T>A	ENSP00000008527.5:n.684+51T>A
ENST00000546722.1:n.177+51T>A
ENST00000552790.5:n.1243+51T>A
NM_004075.4:c.684+51T>A	NP_004066.1:n.684+51T>A
XM_011537939.1:c.600+51T>A	XP_011536241.1:n.600+51T>A
XM_017018832.2:c.600+51T>A	XP_016874321.1:n.600+51T>A
XM_024448844.1:c.684+51T>A	XP_024304612.1:n.684+51T>A
XM_024448845.1:c.600+51T>A	XP_024304613.1:n.600+51T>A
NM_004075.5:c.684+51T>A MANE Select	NP_004066.1:n.684+51T>A