Canonical Allele Identifier: CA607600059

Gene: CRY1

Linked Data

• dbSNP Id: rs1203479945
• gnomAD v2: 12-107395466-AT-A
• gnomAD v3: 12-107001688-AT-A
• gnomAD v4: 12-107001688-AT-A
• MyVariant Identifiers: chr12:g.107395467del (hg19) ; chr12:g.107001689del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.107001690del , CM000674.2:g.107001690del	GRCh38
NC_000012.11:g.107395468del , CM000674.1:g.107395468del	GRCh37
NC_000012.10:g.105919598del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000008527.10:c.595+75del MANE Select	ENSP00000008527.5:n.595+75del
ENST00000008527.9:c.595+75del	ENSP00000008527.5:n.595+75del
ENST00000546722.1:n.88+75del
ENST00000552790.5:n.1154+75del
NM_004075.4:c.595+75del	NP_004066.1:n.595+75del
XM_011537939.1:c.511+75del	XP_011536241.1:n.511+75del
XM_017018832.2:c.511+75del	XP_016874321.1:n.511+75del
XM_024448844.1:c.595+75del	XP_024304612.1:n.595+75del
XM_024448845.1:c.511+75del	XP_024304613.1:n.511+75del
NM_004075.5:c.595+75del MANE Select	NP_004066.1:n.595+75del