Canonical Allele Identifier: CA951511483

Gene: CRY1

Linked Data

• dbSNP Id: rs1952305273
• gnomAD v3: 12-107001208-AAG-A
• gnomAD v4: 12-107001208-AAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.107001214_107001215del , CM000674.2:g.107001214_107001215del	GRCh38
NC_000012.11:g.107394992_107394993del , CM000674.1:g.107394992_107394993del	GRCh37
NC_000012.10:g.105919122_105919123del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000008527.10:c.684+70_684+71del MANE Select	ENSP00000008527.5:n.684+70_684+71del
ENST00000008527.9:c.684+70_684+71del	ENSP00000008527.5:n.684+70_684+71del
ENST00000546722.1:n.177+70_177+71del
ENST00000552790.5:n.1243+70_1243+71del
NM_004075.4:c.684+70_684+71del	NP_004066.1:n.684+70_684+71del
XM_011537939.1:c.600+70_600+71del	XP_011536241.1:n.600+70_600+71del
XM_017018832.2:c.600+70_600+71del	XP_016874321.1:n.600+70_600+71del
XM_024448844.1:c.684+70_684+71del	XP_024304612.1:n.684+70_684+71del
XM_024448845.1:c.600+70_600+71del	XP_024304613.1:n.600+70_600+71del
NM_004075.5:c.684+70_684+71del MANE Select	NP_004066.1:n.684+70_684+71del