Canonical Allele Identifier: CA2259395043

Gene: NR1D1

Linked Data

• dbSNP Id: rs1987816042

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40098871_40098872insCTGCA , CM000679.2:g.40098871_40098872insCTGCA	GRCh38
NC_000017.10:g.38255124_38255125insCTGCA , CM000679.1:g.38255124_38255125insCTGCA	GRCh37
NC_000017.9:g.35508650_35508651insCTGCA	NCBI36
NG_033084.1:g.6858_6859insGTGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246672.4:c.31+1196_31+1197insGTGCA MANE Select	ENSP00000246672.3:n.31+1196_31+1197insGTGCA
ENST00000246672.3:c.31+1196_31+1197insGTGCA	ENSP00000246672.3:n.31+1196_31+1197insGTGCA
NM_021724.4:c.31+1196_31+1197insGTGCA	NP_068370.1:n.31+1196_31+1197insGTGCA
NM_021724.5:c.31+1196_31+1197insGTGCA MANE Select	NP_068370.1:n.31+1196_31+1197insGTGCA