Canonical Allele Identifier: CA1338038985

Gene: PER2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238256691_238256703delinsGACAACTGCCACT , CM000664.2:g.238256691_238256703delinsGACAACTGCCACT	GRCh38
NC_000002.11:g.239165332_239165344delinsGACAACTGCCACT , CM000664.1:g.239165332_239165344delinsGACAACTGCCACT	GRCh37
NC_000002.10:g.238830071_238830083delinsGACAACTGCCACT	NCBI36
NG_012146.1:g.36864_36876delinsAGTGGCAGTTGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707129.1:c.2065+219_2065+231delinsAGTGGCAGTTGTC	ENSP00000516757.1:n.2065+219_2065+231delinsAGTGGCAGTTGTC
ENST00000707130.1:c.2065+219_2065+231delinsAGTGGCAGTTGTC	ENSP00000516758.1:n.2065+219_2065+231delinsAGTGGCAGTTGTC
ENST00000254657.8:c.2065+219_2065+231delinsAGTGGCAGTTGTC MANE Select	ENSP00000254657.3:n.2065+219_2065+231delinsAGTGGCAGTTGTC
ENST00000254657.7:c.2065+219_2065+231delinsAGTGGCAGTTGTC	ENSP00000254657.3:n.2065+219_2065+231delinsAGTGGCAGTTGTC
NM_022817.2:c.2065+219_2065+231delinsAGTGGCAGTTGTC	NP_073728.1:n.2065+219_2065+231delinsAGTGGCAGTTGTC
XM_005246111.3:c.2065+219_2065+231delinsAGTGGCAGTTGTC	XP_005246168.1:n.2065+219_2065+231delinsAGTGGCAGTTGTC
XM_006712824.2:c.2065+219_2065+231delinsAGTGGCAGTTGTC	XP_006712887.1:n.2065+219_2065+231delinsAGTGGCAGTTGTC
XM_005246111.4:c.2065+219_2065+231delinsAGTGGCAGTTGTC	XP_005246168.1:n.2065+219_2065+231delinsAGTGGCAGTTGTC
XM_006712824.4:c.2065+219_2065+231delinsAGTGGCAGTTGTC	XP_006712887.1:n.2065+219_2065+231delinsAGTGGCAGTTGTC
NM_022817.3:c.2065+219_2065+231delinsAGTGGCAGTTGTC MANE Select	NP_073728.1:n.2065+219_2065+231delinsAGTGGCAGTTGTC