Canonical Allele Identifier: CA2620676727

Gene: CRY1

Linked Data

• gnomAD v4: 12-107001328-ACCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.107001329_107001331del , CM000674.2:g.107001329_107001331del	GRCh38
NC_000012.11:g.107395107_107395109del , CM000674.1:g.107395107_107395109del	GRCh37
NC_000012.10:g.105919237_105919239del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000008527.10:c.633_635del MANE Select	ENSP00000008527.5:p.Gly212del
ENST00000008527.9:c.633_635del	ENSP00000008527.5:p.Gly212del
ENST00000546722.1:n.126_128del
ENST00000552790.5:n.1192_1194del
NM_004075.4:c.633_635del	NP_004066.1:p.Gly212del
XM_011537939.1:c.549_551del	XP_011536241.1:p.Gly184del
XM_017018832.2:c.549_551del	XP_016874321.1:p.Gly184del
XM_024448844.1:c.633_635del	XP_024304612.1:p.Gly212del
XM_024448845.1:c.549_551del	XP_024304613.1:p.Gly184del
NM_004075.5:c.633_635del MANE Select	NP_004066.1:p.Gly212del