Canonical Allele Identifier: CA1338049391

Gene: PER2

Linked Data

• dbSNP Id: rs1696501175
• gnomAD v4: 2-238277786-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238277790del , CM000664.2:g.238277790del	GRCh38
NC_000002.11:g.239186431del , CM000664.1:g.239186431del	GRCh37
NC_000002.10:g.238851170del	NCBI36
NG_012146.1:g.15780del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707129.1:c.150del	ENSP00000516757.1:p.Arg51GlyfsTer?
ENST00000707130.1:c.150del	ENSP00000516758.1:p.Arg51GlyfsTer?
ENST00000254657.8:c.150del MANE Select	ENSP00000254657.3:p.Arg51GlyfsTer?
ENST00000254657.7:c.150del	ENSP00000254657.3:p.Arg51GlyfsTer?
ENST00000355768.6:c.150del	ENSP00000348013.2:p.Arg51GlyfsTer?
ENST00000431832.1:c.150del	ENSP00000405891.1:p.Arg51GlyfsTer?
NM_022817.2:c.150del	NP_073728.1:p.Arg51GlyfsTer?
XM_005246111.3:c.150del	XP_005246168.1:p.Arg51GlyfsTer?
XM_006712824.2:c.150del	XP_006712887.1:p.Arg51GlyfsTer?
XM_005246111.4:c.150del	XP_005246168.1:p.Arg51GlyfsTer?
XM_006712824.4:c.150del	XP_006712887.1:p.Arg51GlyfsTer?
NM_022817.3:c.150del MANE Select	NP_073728.1:p.Arg51GlyfsTer?