Canonical Allele Identifier: CA2549600808
Gene: NR1D1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40098985_40098990del , CM000679.2:g.40098985_40098990del GRCh38
NC_000017.10:g.38255238_38255243del , CM000679.1:g.38255238_38255243del GRCh37
NC_000017.9:g.35508764_35508769del NCBI36
NG_033084.1:g.6736_6741del

Transcript Alleles

HGVS Amino-acid Change
ENST00000246672.4:c.31+1074_31+1079del MANE Select ENSP00000246672.3:n.31+1074_31+1079del
ENST00000246672.3:c.31+1074_31+1079del ENSP00000246672.3:n.31+1074_31+1079del
NM_021724.4:c.31+1074_31+1079del NP_068370.1:n.31+1074_31+1079del
NM_021724.5:c.31+1074_31+1079del MANE Select NP_068370.1:n.31+1074_31+1079del