Canonical Allele Identifier: CA2246174391

Gene: PER1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8144851T= , CM000679.2:g.8144851T=	GRCh38
NC_000017.10:g.8048169T= , CM000679.1:g.8048169T=	GRCh37
NC_000017.9:g.7988894T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_002616.3:c.2361A= MANE Select	NP_002607.2:p.Thr787=
ENST00000317276.9:c.2361A= MANE Select	ENSP00000314420.4:p.Thr787=
NM_002616.2:c.2361A=	NP_002607.2:p.Thr787=
ENST00000317276.8:c.2361A=	ENSP00000314420.4:p.Thr787=
ENST00000354903.9:c.2313A=	ENSP00000346979.5:p.Thr771=
ENST00000578089.1:n.298-4A=
ENST00000578950.1:n.320A=
ENST00000581082.5:c.2301A=	ENSP00000462064.1:p.Thr767=
ENST00000581395.5:c.*356A=	ENSP00000464696.1:n.*356A=
ENST00000582719.5:c.2361A=	ENSP00000463054.1:p.Thr787=
ENST00000583559.1:c.210A=	ENSP00000463369.1:p.Thr70=
XM_005256689.1:c.2361A=	XP_005256746.1:p.Thr787=
XM_005256689.2:c.2361A=	XP_005256746.1:p.Thr787=
XM_005256690.1:c.2181A=	XP_005256747.1:p.Thr727=
XM_024450803.1:c.2181A=	XP_024306571.1:p.Thr727=