Canonical Allele Identifier: CA647643606

Gene: PER2

Linked Data

• COSMIC: COSN24309362

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238256829T>A , CM000664.2:g.238256829T>A	GRCh38
NC_000002.11:g.239165470T>A , CM000664.1:g.239165470T>A	GRCh37
NC_000002.10:g.238830209T>A	NCBI36
NG_012146.1:g.36738A>T

Transcript Alleles

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