Canonical Allele Identifier: CA1204410001

Gene: RXRG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419564C= , CM000663.2:g.165419564C=	GRCh38
NC_000001.10:g.165388801C= , CM000663.1:g.165388801C=	GRCh37
NC_000001.9:g.163655425C=	NCBI36
NG_029517.1:g.30792G=
NG_029517.2:g.30792G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.442+306G= MANE Select	ENSP00000352900.5:n.442+306G=
ENST00000359842.9:c.442+306G=	ENSP00000352900.5:n.442+306G=
ENST00000470566.1:n.367+306G=
ENST00000619224.1:c.73+306G=	ENSP00000482458.1:n.73+306G=
NM_001256570.1:c.73+306G=	NP_001243499.1:n.73+306G=
NM_001256571.1:c.73+306G=	NP_001243500.1:n.73+306G=
NM_006917.4:c.442+306G=	NP_008848.1:n.442+306G=
NM_006917.5:c.442+306G= MANE Select	NP_008848.1:n.442+306G=
NM_001256571.2:c.73+306G=	NP_001243500.1:n.73+306G=
NM_001256570.2:c.73+306G=	NP_001243499.1:n.73+306G=