Canonical Allele Identifier: CA2259395109

Gene: NR1D1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40098995_40098997delinsCTT , CM000679.2:g.40098995_40098997delinsCTT	GRCh38
NC_000017.10:g.38255248_38255250delinsCTT , CM000679.1:g.38255248_38255250delinsCTT	GRCh37
NC_000017.9:g.35508774_35508776delinsCTT	NCBI36
NG_033084.1:g.6729_6731delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246672.4:c.31+1067_31+1069delinsAAG MANE Select	ENSP00000246672.3:n.31+1067_31+1069delinsAAG
ENST00000246672.3:c.31+1067_31+1069delinsAAG	ENSP00000246672.3:n.31+1067_31+1069delinsAAG
NM_021724.4:c.31+1067_31+1069delinsAAG	NP_068370.1:n.31+1067_31+1069delinsAAG
NM_021724.5:c.31+1067_31+1069delinsAAG MANE Select	NP_068370.1:n.31+1067_31+1069delinsAAG