Canonical Allele Identifier: CA1396723584

Gene: NR1I2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119807561_119807562delinsCA , CM000665.2:g.119807561_119807562delinsCA	GRCh38
NC_000003.11:g.119526408_119526409delinsCA , CM000665.1:g.119526408_119526409delinsCA	GRCh37
NC_000003.10:g.121009098_121009099delinsCA	NCBI36
NG_011856.1:g.32078_32079delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393716.8:c.197+114_197+115delinsCA MANE Select	ENSP00000377319.3:n.197+114_197+115delinsCA
ENST00000466380.6:c.197+114_197+115delinsCA	ENSP00000420297.2:n.197+114_197+115delinsCA
ENST00000648112.1:c.*334_*335delinsCA	ENSP00000497876.1:n.*334_*335delinsCA
ENST00000337940.4:c.314+114_314+115delinsCA	ENSP00000336528.4:n.314+114_314+115delinsCA
ENST00000393716.6:c.197+114_197+115delinsCA	ENSP00000377319.2:n.197+114_197+115delinsCA
ENST00000466380.5:c.197+114_197+115delinsCA	ENSP00000420297.1:n.197+114_197+115delinsCA
ENST00000474090.1:n.485+114_485+115delinsCA
NM_003889.3:c.197+114_197+115delinsCA	NP_003880.3:n.197+114_197+115delinsCA
NM_022002.2:c.314+114_314+115delinsCA	NP_071285.1:n.314+114_314+115delinsCA
NM_033013.2:c.197+114_197+115delinsCA	NP_148934.1:n.197+114_197+115delinsCA
NM_003889.4:c.197+114_197+115delinsCA MANE Select	NP_003880.3:n.197+114_197+115delinsCA
NM_022002.3:c.314+114_314+115delinsCA	NP_071285.1:n.314+114_314+115delinsCA
NM_033013.3:c.197+114_197+115delinsCA	NP_148934.1:n.197+114_197+115delinsCA