Canonical Allele Identifier: CA386404867

Gene: CRY1

Linked Data

• MyVariant Identifiers: chr12:g.107395100T>G (hg19) ; chr12:g.107001322T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.107001322T>G , CM000674.2:g.107001322T>G	GRCh38
NC_000012.11:g.107395100T>G , CM000674.1:g.107395100T>G	GRCh37
NC_000012.10:g.105919230T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000008527.10:c.642A>C MANE Select	ENSP00000008527.5:p.Glu214Asp
ENST00000008527.9:c.642A>C	ENSP00000008527.5:p.Glu214Asp
ENST00000546722.1:n.135A>C
ENST00000552790.5:n.1201A>C
NM_004075.4:c.642A>C	NP_004066.1:p.Glu214Asp
XM_011537939.1:c.558A>C	XP_011536241.1:p.Glu186Asp
XM_017018832.2:c.558A>C	XP_016874321.1:p.Glu186Asp
XM_024448844.1:c.642A>C	XP_024304612.1:p.Glu214Asp
XM_024448845.1:c.558A>C	XP_024304613.1:p.Glu186Asp
NM_004075.5:c.642A>C MANE Select	NP_004066.1:p.Glu214Asp