Canonical Allele Identifier: CA1338049462

Gene: PER2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238277952G= , CM000664.2:g.238277952G=	GRCh38
NC_000002.11:g.239186593G= , CM000664.1:g.239186593G=	GRCh37
NC_000002.10:g.238851332G=	NCBI36
NG_012146.1:g.15615C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000707129.1:c.-16C=	ENSP00000516757.1:n.-16C=
ENST00000707130.1:c.-16C=	ENSP00000516758.1:n.-16C=
ENST00000254657.8:c.-16C= MANE Select	ENSP00000254657.3:n.-16C=
ENST00000254657.7:c.-16C=	ENSP00000254657.3:n.-16C=
ENST00000431832.1:c.-16C=	ENSP00000405891.1:n.-16C=
NM_022817.2:c.-16C=	NP_073728.1:n.-16C=
XM_005246111.3:c.-16C=	XP_005246168.1:n.-16C=
XM_006712824.2:c.-16C=	XP_006712887.1:n.-16C=
XM_005246111.4:c.-16C=	XP_005246168.1:n.-16C=
XM_006712824.4:c.-16C=	XP_006712887.1:n.-16C=
NM_022817.3:c.-16C= MANE Select	NP_073728.1:n.-16C=