Canonical Allele Identifier: CA540496481

Gene: PER2

Linked Data

• gnomAD v2: 2-239182158-TGGA-T
• gnomAD v3: 2-238273517-TGGA-T
• gnomAD v4: 2-238273517-TGGA-T
• MyVariant Identifiers: chr2:g.239182160_239182162del (hg19) ; chr2:g.238273519_238273521del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238273519_238273521del , CM000664.2:g.238273519_238273521del	GRCh38
NC_000002.11:g.239182160_239182162del , CM000664.1:g.239182160_239182162del	GRCh37
NC_000002.10:g.238846899_238846901del	NCBI36
NG_012146.1:g.20047_20049del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707129.1:c.449-329_449-327del	ENSP00000516757.1:n.449-329_449-327del
ENST00000707130.1:c.449-329_449-327del	ENSP00000516758.1:n.449-329_449-327del
ENST00000254657.8:c.449-329_449-327del MANE Select	ENSP00000254657.3:n.449-329_449-327del
ENST00000254657.7:c.449-329_449-327del	ENSP00000254657.3:n.449-329_449-327del
ENST00000355768.6:c.449-329_449-327del	ENSP00000348013.2:n.449-329_449-327del
NM_022817.2:c.449-329_449-327del	NP_073728.1:n.449-329_449-327del
XM_005246111.3:c.449-329_449-327del	XP_005246168.1:n.449-329_449-327del
XM_006712824.2:c.449-329_449-327del	XP_006712887.1:n.449-329_449-327del
XM_005246111.4:c.449-329_449-327del	XP_005246168.1:n.449-329_449-327del
XM_006712824.4:c.449-329_449-327del	XP_006712887.1:n.449-329_449-327del
NM_022817.3:c.449-329_449-327del MANE Select	NP_073728.1:n.449-329_449-327del