Canonical Allele Identifier: CA243251804
Gene: CRY1 HGNC NCBI

Linked Data

dbSNP Id: rs572242172

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.107001166C>A , CM000674.2:g.107001166C>A GRCh38
NC_000012.11:g.107394944C>A , CM000674.1:g.107394944C>A GRCh37
NC_000012.10:g.105919074C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000008527.10:c.684+114G>T MANE Select ENSP00000008527.5:n.684+114G>T
ENST00000008527.9:c.684+114G>T ENSP00000008527.5:n.684+114G>T
ENST00000546722.1:n.177+114G>T
ENST00000552790.5:n.1243+114G>T
NM_004075.4:c.684+114G>T NP_004066.1:n.684+114G>T
XM_011537939.1:c.600+114G>T XP_011536241.1:n.600+114G>T
XM_017018832.2:c.600+114G>T XP_016874321.1:n.600+114G>T
XM_024448844.1:c.684+114G>T XP_024304612.1:n.684+114G>T
XM_024448845.1:c.600+114G>T XP_024304613.1:n.600+114G>T
NM_004075.5:c.684+114G>T MANE Select NP_004066.1:n.684+114G>T