Canonical Allele Identifier: CA766681761

Gene: PER2

Linked Data

• dbSNP Id: rs1386426185
• MyVariant Identifiers: chr2:g.239165529_239165550del (hg19) ; chr2:g.238256888_238256909del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238256888_238256909del , CM000664.2:g.238256888_238256909del	GRCh38
NC_000002.11:g.239165529_239165550del , CM000664.1:g.239165529_239165550del	GRCh37
NC_000002.10:g.238830268_238830289del	NCBI36
NG_012146.1:g.36658_36679del

Transcript Alleles

HGVS	Amino-acid change
ENST00000707129.1:c.2065+13_2065+34del	ENSP00000516757.1:n.2065+13_2065+34del
ENST00000707130.1:c.2065+13_2065+34del	ENSP00000516758.1:n.2065+13_2065+34del
ENST00000254657.8:c.2065+13_2065+34del MANE Select	ENSP00000254657.3:n.2065+13_2065+34del
ENST00000254657.7:c.2065+13_2065+34del	ENSP00000254657.3:n.2065+13_2065+34del
NM_022817.2:c.2065+13_2065+34del	NP_073728.1:n.2065+13_2065+34del
XM_005246111.3:c.2065+13_2065+34del	XP_005246168.1:n.2065+13_2065+34del
XM_006712824.2:c.2065+13_2065+34del	XP_006712887.1:n.2065+13_2065+34del
XM_005246111.4:c.2065+13_2065+34del	XP_005246168.1:n.2065+13_2065+34del
XM_006712824.4:c.2065+13_2065+34del	XP_006712887.1:n.2065+13_2065+34del
NM_022817.3:c.2065+13_2065+34del MANE Select	NP_073728.1:n.2065+13_2065+34del