Canonical Allele Identifier: CA683209586

Gene: CRY1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.106992962T>C , CM000674.2:g.106992962T>C	GRCh38
NC_000012.11:g.107386740T>C , CM000674.1:g.107386740T>C	GRCh37
NC_000012.10:g.105910870T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000008527.10:c.1657+3A>G MANE Select	ENSP00000008527.5:n.1657+3A>G
ENST00000008527.9:c.1657+3A>G	ENSP00000008527.5:n.1657+3A>G
ENST00000549356.1:c.217+3A>G	ENSP00000447738.1:n.217+3A>G
ENST00000552790.5:n.2239A>G
NM_004075.4:c.1657+3A>G	NP_004066.1:n.1657+3A>G
XM_011537939.1:c.1573+3A>G	XP_011536241.1:n.1573+3A>G
XM_017018832.2:c.1573+3A>G	XP_016874321.1:n.1573+3A>G
XM_024448844.1:c.1660A>G	XP_024304612.1:p.Lys554Glu
XM_024448845.1:c.1576A>G	XP_024304613.1:p.Lys526Glu
NM_004075.5:c.1657+3A>G MANE Select	NP_004066.1:n.1657+3A>G