Canonical Allele Identifier: CA2663914850

Gene: PER2

Linked Data

• gnomAD v4: 2-238256991-GCGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238256994_238256996del , CM000664.2:g.238256994_238256996del	GRCh38
NC_000002.11:g.239165635_239165637del , CM000664.1:g.239165635_239165637del	GRCh37
NC_000002.10:g.238830374_238830376del	NCBI36
NG_012146.1:g.36573_36575del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707129.1:c.1993_1995del	ENSP00000516757.1:p.Ser665del
ENST00000707130.1:c.1993_1995del	ENSP00000516758.1:p.Ser665del
ENST00000254657.8:c.1993_1995del MANE Select	ENSP00000254657.3:p.Ser665del
ENST00000254657.7:c.1993_1995del	ENSP00000254657.3:p.Ser665del
NM_022817.2:c.1993_1995del	NP_073728.1:p.Ser665del
XM_005246111.3:c.1993_1995del	XP_005246168.1:p.Ser665del
XM_006712824.2:c.1993_1995del	XP_006712887.1:p.Ser665del
XM_005246111.4:c.1993_1995del	XP_005246168.1:p.Ser665del
XM_006712824.4:c.1993_1995del	XP_006712887.1:p.Ser665del
NM_022817.3:c.1993_1995del MANE Select	NP_073728.1:p.Ser665del