Canonical Allele Identifier: CA771898041
Gene: NR1D1 HGNC NCBI

Linked Data

dbSNP Id: rs1461946378
MyVariant Identifiers: chr17:g.38255268_38255269insG (hg19) chr17:g.40099015_40099016insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40099020dup , CM000679.2:g.40099020dup GRCh38
NC_000017.10:g.38255273dup , CM000679.1:g.38255273dup GRCh37
NC_000017.9:g.35508799dup NCBI36
NG_033084.1:g.6710dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000246672.4:c.31+1048dup MANE Select ENSP00000246672.3:n.31+1048dup
ENST00000246672.3:c.31+1048dup ENSP00000246672.3:n.31+1048dup
NM_021724.4:c.31+1048dup NP_068370.1:n.31+1048dup
NM_021724.5:c.31+1048dup MANE Select NP_068370.1:n.31+1048dup
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Search 100 bp 3'