Canonical Allele Identifier: CA1968643152

Gene: CRY2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45858559C= , CM000673.2:g.45858559C=	GRCh38
NC_000011.9:g.45880110C= , CM000673.1:g.45880110C=	GRCh37
NC_000011.8:g.45836686C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_021117.5:c.325-172C= MANE Select	NP_066940.3:n.325-172C=
ENST00000616080.2:c.325-172C= MANE Select	ENSP00000484684.1:n.325-172C=
NM_001127457.2:c.142-172C=	NP_001120929.1:n.142-172C=
NM_001127457.3:c.142-172C=	NP_001120929.1:n.142-172C=
NM_021117.3:c.388-172C=	NP_066940.2:n.388-172C=
NM_021117.4:c.325-172C=	NP_066940.3:n.325-172C=
ENST00000417225.6:c.142-172C=	ENSP00000397419.2:n.142-172C=
ENST00000443527.6:c.388-172C=	ENSP00000406751.2:n.388-172C=
ENST00000473199.5:n.338-172C=
ENST00000532390.5:n.338-172C=
ENST00000533779.1:n.108-172C=
ENST00000616080.1:c.325-172C=	ENSP00000484684.1:n.325-172C=
ENST00000616623.4:c.388-172C=	ENSP00000478187.1:n.388-172C=