Canonical Allele Identifier: CA2663887670

Gene: PER2

Linked Data

• gnomAD v4: 2-238275842-CCTTTAGTGTTTTTATCAGTTCTTTGTGTGTGTCCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238275847_238275881del , CM000664.2:g.238275847_238275881del	GRCh38
NC_000002.11:g.239184488_239184522del , CM000664.1:g.239184488_239184522del	GRCh37
NC_000002.10:g.238849227_238849261del	NCBI36
NG_012146.1:g.17690_17724del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707129.1:c.314_348del	ENSP00000516757.1:p.Val105GlyfsTer?
ENST00000707130.1:c.314_348del	ENSP00000516758.1:p.Val105GlyfsTer?
ENST00000254657.8:c.314_348del MANE Select	ENSP00000254657.3:p.Val105GlyfsTer?
ENST00000254657.7:c.314_348del	ENSP00000254657.3:p.Val105GlyfsTer?
ENST00000355768.6:c.314_348del	ENSP00000348013.2:p.Val105GlyfsTer?
NM_022817.2:c.314_348del	NP_073728.1:p.Val105GlyfsTer?
XM_005246111.3:c.314_348del	XP_005246168.1:p.Val105GlyfsTer?
XM_006712824.2:c.314_348del	XP_006712887.1:p.Val105GlyfsTer?
XM_005246111.4:c.314_348del	XP_005246168.1:p.Val105GlyfsTer?
XM_006712824.4:c.314_348del	XP_006712887.1:p.Val105GlyfsTer?
NM_022817.3:c.314_348del MANE Select	NP_073728.1:p.Val105GlyfsTer?