Canonical Allele Identifier: CA2836823599

Gene: NR1D1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40099087_40099088insCGG , CM000679.2:g.40099087_40099088insCGG	GRCh38
NC_000017.10:g.38255340_38255341insCGG , CM000679.1:g.38255340_38255341insCGG	GRCh37
NC_000017.9:g.35508866_35508867insCGG	NCBI36
NG_033084.1:g.6638_6639insCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246672.4:c.31+976_31+977insCCG MANE Select	ENSP00000246672.3:n.31+976_31+977insCCG
ENST00000246672.3:c.31+976_31+977insCCG	ENSP00000246672.3:n.31+976_31+977insCCG
NM_021724.4:c.31+976_31+977insCCG	NP_068370.1:n.31+976_31+977insCCG
NM_021724.5:c.31+976_31+977insCCG MANE Select	NP_068370.1:n.31+976_31+977insCCG