Canonical Allele Identifier: CA2259395385

Gene: NR1D1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40099347_40099349delinsCCG , CM000679.2:g.40099347_40099349delinsCCG	GRCh38
NC_000017.10:g.38255600_38255602delinsCCG , CM000679.1:g.38255600_38255602delinsCCG	GRCh37
NC_000017.9:g.35509126_35509128delinsCCG	NCBI36
NG_033084.1:g.6377_6379delinsCGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246672.4:c.31+715_31+717delinsCGG MANE Select	ENSP00000246672.3:n.31+715_31+717delinsCGG
ENST00000246672.3:c.31+715_31+717delinsCGG	ENSP00000246672.3:n.31+715_31+717delinsCGG
NM_021724.4:c.31+715_31+717delinsCGG	NP_068370.1:n.31+715_31+717delinsCGG
NM_021724.5:c.31+715_31+717delinsCGG MANE Select	NP_068370.1:n.31+715_31+717delinsCGG