Canonical Allele Identifier: CA2259395006

Gene: NR1D1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40098812_40098815delinsAAGG , CM000679.2:g.40098812_40098815delinsAAGG	GRCh38
NC_000017.10:g.38255065_38255068delinsAAGG , CM000679.1:g.38255065_38255068delinsAAGG	GRCh37
NC_000017.9:g.35508591_35508594delinsAAGG	NCBI36
NG_033084.1:g.6911_6914delinsCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246672.4:c.31+1249_31+1252delinsCCTT MANE Select	ENSP00000246672.3:n.31+1249_31+1252delinsCCTT
ENST00000246672.3:c.31+1249_31+1252delinsCCTT	ENSP00000246672.3:n.31+1249_31+1252delinsCCTT
NM_021724.4:c.31+1249_31+1252delinsCCTT	NP_068370.1:n.31+1249_31+1252delinsCCTT
NM_021724.5:c.31+1249_31+1252delinsCCTT MANE Select	NP_068370.1:n.31+1249_31+1252delinsCCTT