Canonical Allele Identifier: CA6764256

Gene: CRY1

Linked Data

• dbSNP Id: rs779426662
• ExAC: 12:107395182 G / A
• gnomAD v2: 12-107395182-G-A
• gnomAD v3: 12-107001404-G-A
• gnomAD v4: 12-107001404-G-A
• MyVariant Identifiers: chr12:g.107395182G>A (hg19) ; chr12:g.107001404G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.107001404G>A , CM000674.2:g.107001404G>A	GRCh38
NC_000012.11:g.107395182G>A , CM000674.1:g.107395182G>A	GRCh37
NC_000012.10:g.105919312G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000008527.10:c.596-36C>T MANE Select	ENSP00000008527.5:n.596-36C>T
ENST00000008527.9:c.596-36C>T	ENSP00000008527.5:n.596-36C>T
ENST00000546722.1:n.89-36C>T
ENST00000552790.5:n.1155-36C>T
NM_004075.4:c.596-36C>T	NP_004066.1:n.596-36C>T
XM_011537939.1:c.512-36C>T	XP_011536241.1:n.512-36C>T
XM_017018832.2:c.512-36C>T	XP_016874321.1:n.512-36C>T
XM_024448844.1:c.596-36C>T	XP_024304612.1:n.596-36C>T
XM_024448845.1:c.512-36C>T	XP_024304613.1:n.512-36C>T
NM_004075.5:c.596-36C>T MANE Select	NP_004066.1:n.596-36C>T