Canonical Allele Identifier: CA2620676937

Gene: CRY1

Linked Data

• gnomAD v4: 12-107001764-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.107001765del , CM000674.2:g.107001765del	GRCh38
NC_000012.11:g.107395543del , CM000674.1:g.107395543del	GRCh37
NC_000012.10:g.105919673del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000008527.10:c.594del MANE Select	ENSP00000008527.5:p.Gly199ValfsTer?
ENST00000008527.9:c.594del	ENSP00000008527.5:p.Gly199ValfsTer?
ENST00000546722.1:n.87del
ENST00000552790.5:n.1153del
NM_004075.4:c.594del	NP_004066.1:p.Gly199ValfsTer?
XM_011537939.1:c.510del	XP_011536241.1:p.Gly171ValfsTer?
XM_017018832.2:c.510del	XP_016874321.1:p.Gly171ValfsTer?
XM_024448844.1:c.594del	XP_024304612.1:p.Gly199ValfsTer?
XM_024448845.1:c.510del	XP_024304613.1:p.Gly171ValfsTer?
NM_004075.5:c.594del MANE Select	NP_004066.1:p.Gly199ValfsTer?