Canonical Allele Identifier: CA2577295345
Gene: PER2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238273265del , CM000664.2:g.238273265del GRCh38
NC_000002.11:g.239181906del , CM000664.1:g.239181906del GRCh37
NC_000002.10:g.238846645del NCBI36
NG_012146.1:g.20304del

Transcript Alleles

HGVS Amino-acid change
ENST00000707129.1:c.449-72del ENSP00000516757.1:n.449-72del
ENST00000707130.1:c.449-72del ENSP00000516758.1:n.449-72del
ENST00000254657.8:c.449-72del MANE Select ENSP00000254657.3:n.449-72del
ENST00000254657.7:c.449-72del ENSP00000254657.3:n.449-72del
ENST00000355768.6:c.449-72del ENSP00000348013.2:n.449-72del
NM_022817.2:c.449-72del NP_073728.1:n.449-72del
XM_005246111.3:c.449-72del XP_005246168.1:n.449-72del
XM_006712824.2:c.449-72del XP_006712887.1:n.449-72del
XM_005246111.4:c.449-72del XP_005246168.1:n.449-72del
XM_006712824.4:c.449-72del XP_006712887.1:n.449-72del
NM_022817.3:c.449-72del MANE Select NP_073728.1:n.449-72del
Search 100 bp 5'
Search 100 bp 3'