Canonical Allele Identifier: CA1396723467

Gene: NR1I2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119807294_119807296delinsTAC , CM000665.2:g.119807294_119807296delinsTAC	GRCh38
NC_000003.11:g.119526141_119526143delinsTAC , CM000665.1:g.119526141_119526143delinsTAC	GRCh37
NC_000003.10:g.121008831_121008833delinsTAC	NCBI36
NG_011856.1:g.31811_31813delinsTAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393716.8:c.44_46delinsTAC MANE Select	ENSP00000377319.3:p.Val15=
ENST00000466380.6:c.44_46delinsTAC	ENSP00000420297.2:p.Val15=
ENST00000648112.1:c.*67_*69delinsTAC	ENSP00000497876.1:n.*67_*69delinsTAC
ENST00000337940.4:c.161_163delinsTAC	ENSP00000336528.4:p.Val54=
ENST00000393716.6:c.44_46delinsTAC	ENSP00000377319.2:p.Val15=
ENST00000466380.5:c.44_46delinsTAC	ENSP00000420297.1:p.Val15=
ENST00000474090.1:n.332_334delinsTAC
NM_003889.3:c.44_46delinsTAC	NP_003880.3:p.Val15=
NM_022002.2:c.161_163delinsTAC	NP_071285.1:p.Val54=
NM_033013.2:c.44_46delinsTAC	NP_148934.1:p.Val15=
NM_003889.4:c.44_46delinsTAC MANE Select	NP_003880.3:p.Val15=
NM_022002.3:c.161_163delinsTAC	NP_071285.1:p.Val54=
NM_033013.3:c.44_46delinsTAC	NP_148934.1:p.Val15=