Canonical Allele Identifier: CA983656130
Gene: NR1D1 HGNC NCBI

Linked Data

dbSNP Id: rs1987831171

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40099375_40099376insCGGC , CM000679.2:g.40099375_40099376insCGGC GRCh38
NC_000017.10:g.38255628_38255629insCGGC , CM000679.1:g.38255628_38255629insCGGC GRCh37
NC_000017.9:g.35509154_35509155insCGGC NCBI36
NG_033084.1:g.6350_6351insGCCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000246672.4:c.31+688_31+689insGCCG MANE Select ENSP00000246672.3:n.31+688_31+689insGCCG
ENST00000246672.3:c.31+688_31+689insGCCG ENSP00000246672.3:n.31+688_31+689insGCCG
NM_021724.4:c.31+688_31+689insGCCG NP_068370.1:n.31+688_31+689insGCCG
NM_021724.5:c.31+688_31+689insGCCG MANE Select NP_068370.1:n.31+688_31+689insGCCG