Canonical Allele Identifier: CA2663914782

Gene: PER2

Linked Data

• gnomAD v4: 2-238256807-CCCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238256808_238256810del , CM000664.2:g.238256808_238256810del	GRCh38
NC_000002.11:g.239165449_239165451del , CM000664.1:g.239165449_239165451del	GRCh37
NC_000002.10:g.238830188_238830190del	NCBI36
NG_012146.1:g.36757_36759del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707129.1:c.2065+112_2065+114del	ENSP00000516757.1:n.2065+112_2065+114del
ENST00000707130.1:c.2065+112_2065+114del	ENSP00000516758.1:n.2065+112_2065+114del
ENST00000254657.8:c.2065+112_2065+114del MANE Select	ENSP00000254657.3:n.2065+112_2065+114del
ENST00000254657.7:c.2065+112_2065+114del	ENSP00000254657.3:n.2065+112_2065+114del
NM_022817.2:c.2065+112_2065+114del	NP_073728.1:n.2065+112_2065+114del
XM_005246111.3:c.2065+112_2065+114del	XP_005246168.1:n.2065+112_2065+114del
XM_006712824.2:c.2065+112_2065+114del	XP_006712887.1:n.2065+112_2065+114del
XM_005246111.4:c.2065+112_2065+114del	XP_005246168.1:n.2065+112_2065+114del
XM_006712824.4:c.2065+112_2065+114del	XP_006712887.1:n.2065+112_2065+114del
NM_022817.3:c.2065+112_2065+114del MANE Select	NP_073728.1:n.2065+112_2065+114del