Canonical Allele Identifier: CA2663887253

Gene: PER2

Linked Data

• gnomAD v4: 2-238273288-ATG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238273289_238273290del , CM000664.2:g.238273289_238273290del	GRCh38
NC_000002.11:g.239181930_239181931del , CM000664.1:g.239181930_239181931del	GRCh37
NC_000002.10:g.238846669_238846670del	NCBI36
NG_012146.1:g.20277_20278del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707129.1:c.449-99_449-98del	ENSP00000516757.1:n.449-99_449-98del
ENST00000707130.1:c.449-99_449-98del	ENSP00000516758.1:n.449-99_449-98del
ENST00000254657.8:c.449-99_449-98del MANE Select	ENSP00000254657.3:n.449-99_449-98del
ENST00000254657.7:c.449-99_449-98del	ENSP00000254657.3:n.449-99_449-98del
ENST00000355768.6:c.449-99_449-98del	ENSP00000348013.2:n.449-99_449-98del
NM_022817.2:c.449-99_449-98del	NP_073728.1:n.449-99_449-98del
XM_005246111.3:c.449-99_449-98del	XP_005246168.1:n.449-99_449-98del
XM_006712824.2:c.449-99_449-98del	XP_006712887.1:n.449-99_449-98del
XM_005246111.4:c.449-99_449-98del	XP_005246168.1:n.449-99_449-98del
XM_006712824.4:c.449-99_449-98del	XP_006712887.1:n.449-99_449-98del
NM_022817.3:c.449-99_449-98del MANE Select	NP_073728.1:n.449-99_449-98del