Canonical Allele Identifier: CA2259395008

Gene: NR1D1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40098814_40098816delinsGGA , CM000679.2:g.40098814_40098816delinsGGA	GRCh38
NC_000017.10:g.38255067_38255069delinsGGA , CM000679.1:g.38255067_38255069delinsGGA	GRCh37
NC_000017.9:g.35508593_35508595delinsGGA	NCBI36
NG_033084.1:g.6910_6912delinsTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246672.4:c.31+1248_31+1250delinsTCC MANE Select	ENSP00000246672.3:n.31+1248_31+1250delinsTCC
ENST00000246672.3:c.31+1248_31+1250delinsTCC	ENSP00000246672.3:n.31+1248_31+1250delinsTCC
NM_021724.4:c.31+1248_31+1250delinsTCC	NP_068370.1:n.31+1248_31+1250delinsTCC
NM_021724.5:c.31+1248_31+1250delinsTCC MANE Select	NP_068370.1:n.31+1248_31+1250delinsTCC