Canonical Allele Identifier: CA6764228

Gene: CRY1

Linked Data

• dbSNP Id: rs758182561
• ExAC: 12:107395037 ATATAATCTACAT / A
• gnomAD v2: 12-107395037-ATATAATCTACAT-A
• gnomAD v4: 12-107001259-ATATAATCTACAT-A
• MyVariant Identifiers: chr12:g.107395038_107395049del (hg19) ; chr12:g.107001260_107001271del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.107001263_107001274del , CM000674.2:g.107001263_107001274del	GRCh38
NC_000012.11:g.107395041_107395052del , CM000674.1:g.107395041_107395052del	GRCh37
NC_000012.10:g.105919171_105919182del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000008527.10:c.684+9_684+20del MANE Select	ENSP00000008527.5:n.684+9_684+20del
ENST00000008527.9:c.684+9_684+20del	ENSP00000008527.5:n.684+9_684+20del
ENST00000546722.1:n.177+9_177+20del
ENST00000552790.5:n.1243+9_1243+20del
NM_004075.4:c.684+9_684+20del	NP_004066.1:n.684+9_684+20del
XM_011537939.1:c.600+9_600+20del	XP_011536241.1:n.600+9_600+20del
XM_017018832.2:c.600+9_600+20del	XP_016874321.1:n.600+9_600+20del
XM_024448844.1:c.684+9_684+20del	XP_024304612.1:n.684+9_684+20del
XM_024448845.1:c.600+9_600+20del	XP_024304613.1:n.600+9_600+20del
NM_004075.5:c.684+9_684+20del MANE Select	NP_004066.1:n.684+9_684+20del