Canonical Allele Identifier: CA1883178032

Gene: RXRA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134417615C= , CM000671.2:g.134417615C=	GRCh38
NC_000009.11:g.137309461C= , CM000671.1:g.137309461C=	GRCh37
NC_000009.10:g.136449282C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_002957.6:c.780+288C= MANE Select	NP_002948.1:n.780+288C=
ENST00000481739.2:c.780+288C= MANE Select	ENSP00000419692.1:n.780+288C=
NM_001291920.1:c.699+288C=	NP_001278849.1:n.699+288C=
NM_001291920.2:c.699+288C=	NP_001278849.1:n.699+288C=
NM_001291921.1:c.489+288C=	NP_001278850.1:n.489+288C=
NM_001291921.2:c.489+288C=	NP_001278850.1:n.489+288C=
NM_002957.5:c.780+288C=	NP_002948.1:n.780+288C=
ENST00000356384.4:n.1190+288C=
ENST00000481739.1:c.780+288C=	ENSP00000419692.1:n.780+288C=
ENST00000672570.1:c.699+288C=	ENSP00000500402.1:n.699+288C=