Canonical Allele Identifier: CA983655831
Gene: NR1D1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40099012_40099014dup , CM000679.2:g.40099012_40099014dup GRCh38
NC_000017.10:g.38255265_38255267dup , CM000679.1:g.38255265_38255267dup GRCh37
NC_000017.9:g.35508791_35508793dup NCBI36
NG_033084.1:g.6714_6716dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000246672.4:c.31+1052_31+1054dup MANE Select ENSP00000246672.3:n.31+1052_31+1054dup
ENST00000246672.3:c.31+1052_31+1054dup ENSP00000246672.3:n.31+1052_31+1054dup
NM_021724.4:c.31+1052_31+1054dup NP_068370.1:n.31+1052_31+1054dup
NM_021724.5:c.31+1052_31+1054dup MANE Select NP_068370.1:n.31+1052_31+1054dup