Canonical Allele Identifier: CA916809032

Gene: PER2

Linked Data

• dbSNP Id: rs1574843693

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238256830_238256834del , CM000664.2:g.238256830_238256834del	GRCh38
NC_000002.11:g.239165471_239165475del , CM000664.1:g.239165471_239165475del	GRCh37
NC_000002.10:g.238830210_238830214del	NCBI36
NG_012146.1:g.36734_36738del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707129.1:c.2065+89_2065+93del	ENSP00000516757.1:n.2065+89_2065+93del
ENST00000707130.1:c.2065+89_2065+93del	ENSP00000516758.1:n.2065+89_2065+93del
ENST00000254657.8:c.2065+89_2065+93del MANE Select	ENSP00000254657.3:n.2065+89_2065+93del
ENST00000254657.7:c.2065+89_2065+93del	ENSP00000254657.3:n.2065+89_2065+93del
NM_022817.2:c.2065+89_2065+93del	NP_073728.1:n.2065+89_2065+93del
XM_005246111.3:c.2065+89_2065+93del	XP_005246168.1:n.2065+89_2065+93del
XM_006712824.2:c.2065+89_2065+93del	XP_006712887.1:n.2065+89_2065+93del
XM_005246111.4:c.2065+89_2065+93del	XP_005246168.1:n.2065+89_2065+93del
XM_006712824.4:c.2065+89_2065+93del	XP_006712887.1:n.2065+89_2065+93del
NM_022817.3:c.2065+89_2065+93del MANE Select	NP_073728.1:n.2065+89_2065+93del