Canonical Allele Identifier: CA6764244

Gene: CRY1

Linked Data

• dbSNP Id: rs751759108
• ExAC: 12:107395107 C / T
• gnomAD v2: 12-107395107-C-T
• gnomAD v4: 12-107001329-C-T
• MyVariant Identifiers: chr12:g.107395107C>T (hg19) ; chr12:g.107001329C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.107001329C>T , CM000674.2:g.107001329C>T	GRCh38
NC_000012.11:g.107395107C>T , CM000674.1:g.107395107C>T	GRCh37
NC_000012.10:g.105919237C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000008527.10:c.635G>A MANE Select	ENSP00000008527.5:p.Gly212Asp
ENST00000008527.9:c.635G>A	ENSP00000008527.5:p.Gly212Asp
ENST00000546722.1:n.128G>A
ENST00000552790.5:n.1194G>A
NM_004075.4:c.635G>A	NP_004066.1:p.Gly212Asp
XM_011537939.1:c.551G>A	XP_011536241.1:p.Gly184Asp
XM_017018832.2:c.551G>A	XP_016874321.1:p.Gly184Asp
XM_024448844.1:c.635G>A	XP_024304612.1:p.Gly212Asp
XM_024448845.1:c.551G>A	XP_024304613.1:p.Gly184Asp
NM_004075.5:c.635G>A MANE Select	NP_004066.1:p.Gly212Asp