Canonical Allele Identifier: CA912973384

Gene: CRY1

Linked Data

• MyVariant Identifiers: chr12:g.107395137_107395138insTA (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.107001361_107001362dup , CM000674.2:g.107001361_107001362dup	GRCh38
NC_000012.11:g.107395139_107395140dup , CM000674.1:g.107395139_107395140dup	GRCh37
NC_000012.10:g.105919269_105919270dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000008527.10:c.603_604dup MANE Select	ENSP00000008527.5:p.Thr202IlefsTer?
ENST00000008527.9:c.603_604dup	ENSP00000008527.5:p.Thr202IlefsTer?
ENST00000546722.1:n.96_97dup
ENST00000552790.5:n.1162_1163dup
NM_004075.4:c.603_604dup	NP_004066.1:p.Thr202IlefsTer?
XM_011537939.1:c.519_520dup	XP_011536241.1:p.Thr174IlefsTer?
XM_017018832.2:c.519_520dup	XP_016874321.1:p.Thr174IlefsTer?
XM_024448844.1:c.603_604dup	XP_024304612.1:p.Thr202IlefsTer?
XM_024448845.1:c.519_520dup	XP_024304613.1:p.Thr174IlefsTer?
NM_004075.5:c.603_604dup MANE Select	NP_004066.1:p.Thr202IlefsTer?