Canonical Allele Identifier: CA771898028
Gene: NR1D1 HGNC NCBI

Linked Data

dbSNP Id: rs1258083426
MyVariant Identifiers: chr17:g.38255266_38255267insA (hg19) chr17:g.40099013_40099014insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40099013_40099014insA , CM000679.2:g.40099013_40099014insA GRCh38
NC_000017.10:g.38255266_38255267insA , CM000679.1:g.38255266_38255267insA GRCh37
NC_000017.9:g.35508792_35508793insA NCBI36
NG_033084.1:g.6712_6713insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000246672.4:c.31+1050_31+1051insT MANE Select ENSP00000246672.3:n.31+1050_31+1051insT
ENST00000246672.3:c.31+1050_31+1051insT ENSP00000246672.3:n.31+1050_31+1051insT
NM_021724.4:c.31+1050_31+1051insT NP_068370.1:n.31+1050_31+1051insT
NM_021724.5:c.31+1050_31+1051insT MANE Select NP_068370.1:n.31+1050_31+1051insT
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