Canonical Allele Identifier: CA1043882856

Gene: PER2

Linked Data

• dbSNP Id: rs1696444328
• gnomAD v3: 2-238276015-GCCC-G
• gnomAD v4: 2-238276015-GCCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238276016_238276018del , CM000664.2:g.238276016_238276018del	GRCh38
NC_000002.11:g.239184657_239184659del , CM000664.1:g.239184657_239184659del	GRCh37
NC_000002.10:g.238849396_238849398del	NCBI36
NG_012146.1:g.17549_17551del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707129.1:c.294-121_294-119del	ENSP00000516757.1:n.294-121_294-119del
ENST00000707130.1:c.294-121_294-119del	ENSP00000516758.1:n.294-121_294-119del
ENST00000254657.8:c.294-121_294-119del MANE Select	ENSP00000254657.3:n.294-121_294-119del
ENST00000254657.7:c.294-121_294-119del	ENSP00000254657.3:n.294-121_294-119del
ENST00000355768.6:c.294-121_294-119del	ENSP00000348013.2:n.294-121_294-119del
ENST00000431832.1:c.294-121_294-119del	ENSP00000405891.1:n.294-121_294-119del
NM_022817.2:c.294-121_294-119del	NP_073728.1:n.294-121_294-119del
XM_005246111.3:c.294-121_294-119del	XP_005246168.1:n.294-121_294-119del
XM_006712824.2:c.294-121_294-119del	XP_006712887.1:n.294-121_294-119del
XM_005246111.4:c.294-121_294-119del	XP_005246168.1:n.294-121_294-119del
XM_006712824.4:c.294-121_294-119del	XP_006712887.1:n.294-121_294-119del
NM_022817.3:c.294-121_294-119del MANE Select	NP_073728.1:n.294-121_294-119del