Canonical Allele Identifier: CA2246150935

Gene: PER1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8149767T= , CM000679.2:g.8149767T=	GRCh38
NC_000017.10:g.8053085T= , CM000679.1:g.8053085T=	GRCh37
NC_000017.9:g.7993810T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_002616.3:c.639A= MANE Select	NP_002607.2:p.Thr213=
ENST00000317276.9:c.639A= MANE Select	ENSP00000314420.4:p.Thr213=
NM_002616.2:c.639A=	NP_002607.2:p.Thr213=
ENST00000317276.8:c.639A=	ENSP00000314420.4:p.Thr213=
ENST00000354903.9:c.591A=	ENSP00000346979.5:p.Thr197=
ENST00000579065.1:n.825A=
ENST00000581082.5:c.639A=	ENSP00000462064.1:p.Thr213=
ENST00000581395.5:c.639A=	ENSP00000464696.1:p.Thr213=
ENST00000582719.5:c.639A=	ENSP00000463054.1:p.Thr213=
XM_005256689.1:c.639A=	XP_005256746.1:p.Thr213=
XM_005256689.2:c.639A=	XP_005256746.1:p.Thr213=
XM_005256690.1:c.639A=	XP_005256747.1:p.Thr213=
XM_024450803.1:c.639A=	XP_024306571.1:p.Thr213=