Canonical Allele Identifier: CA386404955

Gene: CRY1

Linked Data

• MyVariant Identifiers: chr12:g.107395111G>A (hg19) ; chr12:g.107001333G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.107001333G>A , CM000674.2:g.107001333G>A	GRCh38
NC_000012.11:g.107395111G>A , CM000674.1:g.107395111G>A	GRCh37
NC_000012.10:g.105919241G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000008527.10:c.631C>T MANE Select	ENSP00000008527.5:p.Pro211Ser
ENST00000008527.9:c.631C>T	ENSP00000008527.5:p.Pro211Ser
ENST00000546722.1:n.124C>T
ENST00000552790.5:n.1190C>T
NM_004075.4:c.631C>T	NP_004066.1:p.Pro211Ser
XM_011537939.1:c.547C>T	XP_011536241.1:p.Pro183Ser
XM_017018832.2:c.547C>T	XP_016874321.1:p.Pro183Ser
XM_024448844.1:c.631C>T	XP_024304612.1:p.Pro211Ser
XM_024448845.1:c.547C>T	XP_024304613.1:p.Pro183Ser
NM_004075.5:c.631C>T MANE Select	NP_004066.1:p.Pro211Ser