Canonical Allele Identifier: CA1338039092

Gene: PER2

Linked Data

• dbSNP Id: rs1695775250
• gnomAD v4: 2-238256810-TATCGGGCTATGGTGGAGTTCTTCTGCACTTAGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238256812_238256844del , CM000664.2:g.238256812_238256844del	GRCh38
NC_000002.11:g.239165453_239165485del , CM000664.1:g.239165453_239165485del	GRCh37
NC_000002.10:g.238830192_238830224del	NCBI36
NG_012146.1:g.36724_36756del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707129.1:c.2065+79_2065+111del	ENSP00000516757.1:n.2065+79_2065+111del
ENST00000707130.1:c.2065+79_2065+111del	ENSP00000516758.1:n.2065+79_2065+111del
ENST00000254657.8:c.2065+79_2065+111del MANE Select	ENSP00000254657.3:n.2065+79_2065+111del
ENST00000254657.7:c.2065+79_2065+111del	ENSP00000254657.3:n.2065+79_2065+111del
NM_022817.2:c.2065+79_2065+111del	NP_073728.1:n.2065+79_2065+111del
XM_005246111.3:c.2065+79_2065+111del	XP_005246168.1:n.2065+79_2065+111del
XM_006712824.2:c.2065+79_2065+111del	XP_006712887.1:n.2065+79_2065+111del
XM_005246111.4:c.2065+79_2065+111del	XP_005246168.1:n.2065+79_2065+111del
XM_006712824.4:c.2065+79_2065+111del	XP_006712887.1:n.2065+79_2065+111del
NM_022817.3:c.2065+79_2065+111del MANE Select	NP_073728.1:n.2065+79_2065+111del