Canonical Allele Identifier: CA2667141648

Gene: NR1I2

Linked Data

• gnomAD v4: 3-119807297-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119807298del , CM000665.2:g.119807298del	GRCh38
NC_000003.11:g.119526145del , CM000665.1:g.119526145del	GRCh37
NC_000003.10:g.121008835del	NCBI36
NG_011856.1:g.31815del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393716.8:c.48del MANE Select	ENSP00000377319.3:p.Cys17ValfsTer?
ENST00000466380.6:c.48del	ENSP00000420297.2:p.Cys17ValfsTer?
ENST00000648112.1:c.*71del	ENSP00000497876.1:n.*71del
ENST00000337940.4:c.165del	ENSP00000336528.4:p.Cys56ValfsTer?
ENST00000393716.6:c.48del	ENSP00000377319.2:p.Cys17ValfsTer?
ENST00000466380.5:c.48del	ENSP00000420297.1:p.Cys17ValfsTer?
ENST00000474090.1:n.336del
NM_003889.3:c.48del	NP_003880.3:p.Cys17ValfsTer?
NM_022002.2:c.165del	NP_071285.1:p.Cys56ValfsTer?
NM_033013.2:c.48del	NP_148934.1:p.Cys17ValfsTer?
NM_003889.4:c.48del MANE Select	NP_003880.3:p.Cys17ValfsTer?
NM_022002.3:c.165del	NP_071285.1:p.Cys56ValfsTer?
NM_033013.3:c.48del	NP_148934.1:p.Cys17ValfsTer?