Canonical Allele Identifier: CA1338047133
Gene: PER2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238273143_238273144delinsCA , CM000664.2:g.238273143_238273144delinsCA GRCh38
NC_000002.11:g.239181784_239181785delinsCA , CM000664.1:g.239181784_239181785delinsCA GRCh37
NC_000002.10:g.238846523_238846524delinsCA NCBI36
NG_012146.1:g.20423_20424delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000707129.1:c.496_497delinsTG ENSP00000516757.1:p.Cys166=
ENST00000707130.1:c.496_497delinsTG ENSP00000516758.1:p.Cys166=
ENST00000254657.8:c.496_497delinsTG MANE Select ENSP00000254657.3:p.Cys166=
ENST00000254657.7:c.496_497delinsTG ENSP00000254657.3:p.Cys166=
ENST00000355768.6:c.496_497delinsTG ENSP00000348013.2:p.Cys166=
NM_022817.2:c.496_497delinsTG NP_073728.1:p.Cys166=
XM_005246111.3:c.496_497delinsTG XP_005246168.1:p.Cys166=
XM_006712824.2:c.496_497delinsTG XP_006712887.1:p.Cys166=
XM_005246111.4:c.496_497delinsTG XP_005246168.1:p.Cys166=
XM_006712824.4:c.496_497delinsTG XP_006712887.1:p.Cys166=
NM_022817.3:c.496_497delinsTG MANE Select NP_073728.1:p.Cys166=
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Search 100 bp 3'