Canonical Allele Identifier: CA386404992

Gene: CRY1

Linked Data

• MyVariant Identifiers: chr12:g.107395114A>C (hg19) ; chr12:g.107001336A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.107001336A>C , CM000674.2:g.107001336A>C	GRCh38
NC_000012.11:g.107395114A>C , CM000674.1:g.107395114A>C	GRCh37
NC_000012.10:g.105919244A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000008527.10:c.628T>G MANE Select	ENSP00000008527.5:p.Trp210Gly
ENST00000008527.9:c.628T>G	ENSP00000008527.5:p.Trp210Gly
ENST00000546722.1:n.121T>G
ENST00000552790.5:n.1187T>G
NM_004075.4:c.628T>G	NP_004066.1:p.Trp210Gly
XM_011537939.1:c.544T>G	XP_011536241.1:p.Trp182Gly
XM_017018832.2:c.544T>G	XP_016874321.1:p.Trp182Gly
XM_024448844.1:c.628T>G	XP_024304612.1:p.Trp210Gly
XM_024448845.1:c.544T>G	XP_024304613.1:p.Trp182Gly
NM_004075.5:c.628T>G MANE Select	NP_004066.1:p.Trp210Gly