Canonical Allele Identifier: CA2620676730

Gene: CRY1

Linked Data

• gnomAD v4: 12-107001368-C-CTT

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.107001368_107001369insTT , CM000674.2:g.107001368_107001369insTT	GRCh38
NC_000012.11:g.107395146_107395147insTT , CM000674.1:g.107395146_107395147insTT	GRCh37
NC_000012.10:g.105919276_105919277insTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000008527.10:c.596-1_596insAA MANE Select	ENSP00000008527.5:n.596-1_596insAA
ENST00000008527.9:c.596-1_596insAA	ENSP00000008527.5:n.596-1_596insAA
ENST00000546722.1:n.89-1_89insAA
ENST00000552790.5:n.1155-1_1155insAA
NM_004075.4:c.596-1_596insAA	NP_004066.1:n.596-1_596insAA
XM_011537939.1:c.512-1_512insAA	XP_011536241.1:n.512-1_512insAA
XM_017018832.2:c.512-1_512insAA	XP_016874321.1:n.512-1_512insAA
XM_024448844.1:c.596-1_596insAA	XP_024304612.1:n.596-1_596insAA
XM_024448845.1:c.512-1_512insAA	XP_024304613.1:n.512-1_512insAA
NM_004075.5:c.596-1_596insAA MANE Select	NP_004066.1:n.596-1_596insAA