Canonical Allele Identifier: CA771898027
Gene: NR1D1 HGNC NCBI

Linked Data

dbSNP Id: rs1440446309
MyVariant Identifiers: chr17:g.38255263_38255264insC (hg19) chr17:g.40099010_40099011insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40099010_40099011insC , CM000679.2:g.40099010_40099011insC GRCh38
NC_000017.10:g.38255263_38255264insC , CM000679.1:g.38255263_38255264insC GRCh37
NC_000017.9:g.35508789_35508790insC NCBI36
NG_033084.1:g.6715_6716insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000246672.4:c.31+1053_31+1054insG MANE Select ENSP00000246672.3:n.31+1053_31+1054insG
ENST00000246672.3:c.31+1053_31+1054insG ENSP00000246672.3:n.31+1053_31+1054insG
NM_021724.4:c.31+1053_31+1054insG NP_068370.1:n.31+1053_31+1054insG
NM_021724.5:c.31+1053_31+1054insG MANE Select NP_068370.1:n.31+1053_31+1054insG
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