Canonical Allele Identifier: CA771898357
Gene: NR1D1 HGNC NCBI

Linked Data

dbSNP Id: rs1446045111
MyVariant Identifiers: chr17:g.38255567_38255571del (hg19) chr17:g.40099314_40099318del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40099317_40099321del , CM000679.2:g.40099317_40099321del GRCh38
NC_000017.10:g.38255570_38255574del , CM000679.1:g.38255570_38255574del GRCh37
NC_000017.9:g.35509096_35509100del NCBI36
NG_033084.1:g.6408_6412del

Transcript Alleles

HGVS Amino-acid Change
ENST00000246672.4:c.31+746_31+750del MANE Select ENSP00000246672.3:n.31+746_31+750del
ENST00000246672.3:c.31+746_31+750del ENSP00000246672.3:n.31+746_31+750del
NM_021724.4:c.31+746_31+750del NP_068370.1:n.31+746_31+750del
NM_021724.5:c.31+746_31+750del MANE Select NP_068370.1:n.31+746_31+750del
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