Canonical Allele Identifier: CA2577909381

Gene: NR1I2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119807183_119807184del , CM000665.2:g.119807183_119807184del	GRCh38
NC_000003.11:g.119526030_119526031del , CM000665.1:g.119526030_119526031del	GRCh37
NC_000003.10:g.121008720_121008721del	NCBI36
NG_011856.1:g.31700_31701del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393716.8:c.-22-46_-22-45del MANE Select	ENSP00000377319.3:n.-22-46_-22-45del
ENST00000466380.6:c.-22-46_-22-45del	ENSP00000420297.2:n.-22-46_-22-45del
ENST00000648112.1:c.*2-46_*2-45del	ENSP00000497876.1:n.*2-46_*2-45del
ENST00000337940.4:c.96-46_96-45del	ENSP00000336528.4:n.96-46_96-45del
ENST00000393716.6:c.-22-46_-22-45del	ENSP00000377319.2:n.-22-46_-22-45del
ENST00000466380.5:c.-22-46_-22-45del	ENSP00000420297.1:n.-22-46_-22-45del
ENST00000474090.1:n.267-46_267-45del
NM_003889.3:c.-22-46_-22-45del	NP_003880.3:n.-22-46_-22-45del
NM_022002.2:c.96-46_96-45del	NP_071285.1:n.96-46_96-45del
NM_033013.2:c.-22-46_-22-45del	NP_148934.1:n.-22-46_-22-45del
NM_003889.4:c.-22-46_-22-45del MANE Select	NP_003880.3:n.-22-46_-22-45del
NM_022002.3:c.96-46_96-45del	NP_071285.1:n.96-46_96-45del
NM_033013.3:c.-22-46_-22-45del	NP_148934.1:n.-22-46_-22-45del