Canonical Allele Identifier: CA1883176821

Gene: RXRA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408292C= , CM000671.2:g.134408292C=	GRCh38
NC_000009.11:g.137300138C= , CM000671.1:g.137300138C=	GRCh37
NC_000009.10:g.136439959C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.423C= MANE Select	ENSP00000419692.1:p.Arg141=
ENST00000672570.1:c.342C=	ENSP00000500402.1:p.Arg114=
ENST00000356384.4:n.833C=
ENST00000481739.1:c.423C=	ENSP00000419692.1:p.Arg141=
NM_001291920.1:c.342C=	NP_001278849.1:p.Arg114=
NM_001291921.1:c.132C=	NP_001278850.1:p.Arg44=
NM_002957.5:c.423C=	NP_002948.1:p.Arg141=
NM_002957.6:c.423C= MANE Select	NP_002948.1:p.Arg141=
NM_001291921.2:c.132C=	NP_001278850.1:p.Arg44=
NM_001291920.2:c.342C=	NP_001278849.1:p.Arg114=