Canonical Allele Identifier: CA771897955
Gene: NR1D1 HGNC NCBI

Linked Data

dbSNP Id: rs1433232448
MyVariant Identifiers: chr17:g.38255176_38255177insAAC (hg19) chr17:g.40098923_40098924insAAC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40098923_40098924insAAC , CM000679.2:g.40098923_40098924insAAC GRCh38
NC_000017.10:g.38255176_38255177insAAC , CM000679.1:g.38255176_38255177insAAC GRCh37
NC_000017.9:g.35508702_35508703insAAC NCBI36
NG_033084.1:g.6802_6803insGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000246672.4:c.31+1140_31+1141insGTT MANE Select ENSP00000246672.3:n.31+1140_31+1141insGTT
ENST00000246672.3:c.31+1140_31+1141insGTT ENSP00000246672.3:n.31+1140_31+1141insGTT
NM_021724.4:c.31+1140_31+1141insGTT NP_068370.1:n.31+1140_31+1141insGTT
NM_021724.5:c.31+1140_31+1141insGTT MANE Select NP_068370.1:n.31+1140_31+1141insGTT
Search 100 bp 5'
Search 100 bp 3'