Canonical Allele Identifier: CA766700239

Gene: PER2

Linked Data

• dbSNP Id: rs1423304132
• MyVariant Identifiers: chr2:g.239186606_239186607del (hg19) ; chr2:g.238277965_238277966del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238277967_238277968del , CM000664.2:g.238277967_238277968del	GRCh38
NC_000002.11:g.239186608_239186609del , CM000664.1:g.239186608_239186609del	GRCh37
NC_000002.10:g.238851347_238851348del	NCBI36
NG_012146.1:g.15601_15602del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707129.1:c.-19-11_-19-10del	ENSP00000516757.1:n.-19-11_-19-10del
ENST00000707130.1:c.-19-11_-19-10del	ENSP00000516758.1:n.-19-11_-19-10del
ENST00000254657.8:c.-19-11_-19-10del MANE Select	ENSP00000254657.3:n.-19-11_-19-10del
ENST00000254657.7:c.-19-11_-19-10del	ENSP00000254657.3:n.-19-11_-19-10del
ENST00000431832.1:c.-19-11_-19-10del	ENSP00000405891.1:n.-19-11_-19-10del
NM_022817.2:c.-19-11_-19-10del	NP_073728.1:n.-19-11_-19-10del
XM_005246111.3:c.-19-11_-19-10del	XP_005246168.1:n.-19-11_-19-10del
XM_006712824.2:c.-19-11_-19-10del	XP_006712887.1:n.-19-11_-19-10del
XM_005246111.4:c.-19-11_-19-10del	XP_005246168.1:n.-19-11_-19-10del
XM_006712824.4:c.-19-11_-19-10del	XP_006712887.1:n.-19-11_-19-10del
NM_022817.3:c.-19-11_-19-10del MANE Select	NP_073728.1:n.-19-11_-19-10del