Canonical Allele Identifier: CA2841991326

Gene: PER2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238277893del , CM000664.2:g.238277893del	GRCh38
NC_000002.11:g.239186534del , CM000664.1:g.239186534del	GRCh37
NC_000002.10:g.238851273del	NCBI36
NG_012146.1:g.15675del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707129.1:c.45del	ENSP00000516757.1:p.Lys16ArgfsTer19
ENST00000707130.1:c.45del	ENSP00000516758.1:p.Lys16ArgfsTer19
ENST00000254657.8:c.45del MANE Select	ENSP00000254657.3:p.Lys16ArgfsTer19
ENST00000254657.7:c.45del	ENSP00000254657.3:p.Lys16ArgfsTer19
ENST00000355768.6:c.45del	ENSP00000348013.2:p.Lys16ArgfsTer19
ENST00000431832.1:c.45del	ENSP00000405891.1:p.Lys16ArgfsTer19
NM_022817.2:c.45del	NP_073728.1:p.Lys16ArgfsTer19
XM_005246111.3:c.45del	XP_005246168.1:p.Lys16ArgfsTer19
XM_006712824.2:c.45del	XP_006712887.1:p.Lys16ArgfsTer19
XM_005246111.4:c.45del	XP_005246168.1:p.Lys16ArgfsTer19
XM_006712824.4:c.45del	XP_006712887.1:p.Lys16ArgfsTer19
NM_022817.3:c.45del MANE Select	NP_073728.1:p.Lys16ArgfsTer19