Canonical Allele Identifier: CA1396723262

Gene: NR1I2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119806947_119806949delinsCTT , CM000665.2:g.119806947_119806949delinsCTT	GRCh38
NC_000003.11:g.119525794_119525796delinsCTT , CM000665.1:g.119525794_119525796delinsCTT	GRCh37
NC_000003.10:g.121008484_121008486delinsCTT	NCBI36
NG_011856.1:g.31464_31466delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393716.8:c.-22-282_-22-280delinsCTT MANE Select	ENSP00000377319.3:n.-22-282_-22-280delinsCTT
ENST00000466380.6:c.-22-282_-22-280delinsCTT	ENSP00000420297.2:n.-22-282_-22-280delinsCTT
ENST00000648112.1:c.*2-282_*2-280delinsCTT	ENSP00000497876.1:n.*2-282_*2-280delinsCTT
ENST00000337940.4:c.96-282_96-280delinsCTT	ENSP00000336528.4:n.96-282_96-280delinsCTT
ENST00000393716.6:c.-22-282_-22-280delinsCTT	ENSP00000377319.2:n.-22-282_-22-280delinsCTT
ENST00000466380.5:c.-22-282_-22-280delinsCTT	ENSP00000420297.1:n.-22-282_-22-280delinsCTT
ENST00000474090.1:n.267-282_267-280delinsCTT
NM_003889.3:c.-22-282_-22-280delinsCTT	NP_003880.3:n.-22-282_-22-280delinsCTT
NM_022002.2:c.96-282_96-280delinsCTT	NP_071285.1:n.96-282_96-280delinsCTT
NM_033013.2:c.-22-282_-22-280delinsCTT	NP_148934.1:n.-22-282_-22-280delinsCTT
NM_003889.4:c.-22-282_-22-280delinsCTT MANE Select	NP_003880.3:n.-22-282_-22-280delinsCTT
NM_022002.3:c.96-282_96-280delinsCTT	NP_071285.1:n.96-282_96-280delinsCTT
NM_033013.3:c.-22-282_-22-280delinsCTT	NP_148934.1:n.-22-282_-22-280delinsCTT