Canonical Allele Identifier: CA1338047114

Gene: PER2

Linked Data

• dbSNP Id: rs1696341899

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238273113_238273115del , CM000664.2:g.238273113_238273115del	GRCh38
NC_000002.11:g.239181754_239181756del , CM000664.1:g.239181754_239181756del	GRCh37
NC_000002.10:g.238846493_238846495del	NCBI36
NG_012146.1:g.20456_20458del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707129.1:c.529_531del	ENSP00000516757.1:p.Glu177del
ENST00000707130.1:c.529_531del	ENSP00000516758.1:p.Glu177del
ENST00000254657.8:c.529_531del MANE Select	ENSP00000254657.3:p.Glu177del
ENST00000254657.7:c.529_531del	ENSP00000254657.3:p.Glu177del
ENST00000355768.6:c.529_531del	ENSP00000348013.2:p.Glu177del
NM_022817.2:c.529_531del	NP_073728.1:p.Glu177del
XM_005246111.3:c.529_531del	XP_005246168.1:p.Glu177del
XM_006712824.2:c.529_531del	XP_006712887.1:p.Glu177del
XM_005246111.4:c.529_531del	XP_005246168.1:p.Glu177del
XM_006712824.4:c.529_531del	XP_006712887.1:p.Glu177del
NM_022817.3:c.529_531del MANE Select	NP_073728.1:p.Glu177del