Canonical Allele Identifier: CA2663887088
Gene: PER2 HGNC NCBI

Linked Data

gnomAD v4: 2-238273175-G-GTAA
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238273178_238273180dup , CM000664.2:g.238273178_238273180dup GRCh38
NC_000002.11:g.239181819_239181821dup , CM000664.1:g.239181819_239181821dup GRCh37
NC_000002.10:g.238846558_238846560dup NCBI36
NG_012146.1:g.20389_20391dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000707129.1:c.462_464dup ENSP00000516757.1:p.Tyr155_Gln156insTyr
ENST00000707130.1:c.462_464dup ENSP00000516758.1:p.Tyr155_Gln156insTyr
ENST00000254657.8:c.462_464dup MANE Select ENSP00000254657.3:p.Tyr155_Gln156insTyr
ENST00000254657.7:c.462_464dup ENSP00000254657.3:p.Tyr155_Gln156insTyr
ENST00000355768.6:c.462_464dup ENSP00000348013.2:p.Tyr155_Gln156insTyr
NM_022817.2:c.462_464dup NP_073728.1:p.Tyr155_Gln156insTyr
XM_005246111.3:c.462_464dup XP_005246168.1:p.Tyr155_Gln156insTyr
XM_006712824.2:c.462_464dup XP_006712887.1:p.Tyr155_Gln156insTyr
XM_005246111.4:c.462_464dup XP_005246168.1:p.Tyr155_Gln156insTyr
XM_006712824.4:c.462_464dup XP_006712887.1:p.Tyr155_Gln156insTyr
NM_022817.3:c.462_464dup MANE Select NP_073728.1:p.Tyr155_Gln156insTyr
Search 100 bp 5'
Search 100 bp 3'