Canonical Allele Identifier: CA398019902

Gene: PER1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8152405A>T , CM000679.2:g.8152405A>T	GRCh38
NC_000017.10:g.8055723A>T , CM000679.1:g.8055723A>T	GRCh37
NC_000017.9:g.7996448A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317276.8:c.-208T>A	ENSP00000314420.4:n.-208T>A
ENST00000354903.9:c.49-1795T>A	ENSP00000346979.5:n.49-1795T>A
ENST00000498285.1:c.335-1560T>A	ENSP00000464383.1:n.335-1560T>A
ENST00000577253.5:c.-139-1560T>A	ENSP00000462546.1:n.-139-1560T>A
ENST00000581395.5:c.-139-1560T>A	ENSP00000464696.1:n.-139-1560T>A
ENST00000581703.1:c.28T>A	ENSP00000463385.1:p.Trp10Arg
ENST00000584202.1:c.-140+1525T>A	ENSP00000463661.1:n.-140+1525T>A
NM_002616.2:c.-208T>A	NP_002607.2:n.-208T>A
XM_005256689.1:c.-139-1560T>A	XP_005256746.1:n.-139-1560T>A
XM_005256690.1:c.-208T>A	XP_005256747.1:n.-208T>A
XM_005256689.2:c.-139-1560T>A	XP_005256746.1:n.-139-1560T>A
XM_024450803.1:c.-139-1560T>A	XP_024306571.1:n.-139-1560T>A