Canonical Allele Identifier: CA1338047243

Gene: PER2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238273378_238273379delinsTA , CM000664.2:g.238273378_238273379delinsTA	GRCh38
NC_000002.11:g.239182019_239182020delinsTA , CM000664.1:g.239182019_239182020delinsTA	GRCh37
NC_000002.10:g.238846758_238846759delinsTA	NCBI36
NG_012146.1:g.20188_20189delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707129.1:c.449-188_449-187delinsTA	ENSP00000516757.1:n.449-188_449-187delinsTA
ENST00000707130.1:c.449-188_449-187delinsTA	ENSP00000516758.1:n.449-188_449-187delinsTA
ENST00000254657.8:c.449-188_449-187delinsTA MANE Select	ENSP00000254657.3:n.449-188_449-187delinsTA
ENST00000254657.7:c.449-188_449-187delinsTA	ENSP00000254657.3:n.449-188_449-187delinsTA
ENST00000355768.6:c.449-188_449-187delinsTA	ENSP00000348013.2:n.449-188_449-187delinsTA
NM_022817.2:c.449-188_449-187delinsTA	NP_073728.1:n.449-188_449-187delinsTA
XM_005246111.3:c.449-188_449-187delinsTA	XP_005246168.1:n.449-188_449-187delinsTA
XM_006712824.2:c.449-188_449-187delinsTA	XP_006712887.1:n.449-188_449-187delinsTA
XM_005246111.4:c.449-188_449-187delinsTA	XP_005246168.1:n.449-188_449-187delinsTA
XM_006712824.4:c.449-188_449-187delinsTA	XP_006712887.1:n.449-188_449-187delinsTA
NM_022817.3:c.449-188_449-187delinsTA MANE Select	NP_073728.1:n.449-188_449-187delinsTA