Canonical Allele Identifier: CA1204419849

Gene: RXRG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165439955_165439958delinsGAGA , CM000663.2:g.165439955_165439958delinsGAGA	GRCh38
NC_000001.10:g.165409192_165409195delinsGAGA , CM000663.1:g.165409192_165409195delinsGAGA	GRCh37
NC_000001.9:g.163675816_163675819delinsGAGA	NCBI36
NG_029517.1:g.10398_10401delinsTCTC
NG_029517.2:g.10398_10401delinsTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.49+4887_49+4890delinsTCTC MANE Select	ENSP00000352900.5:n.49+4887_49+4890delinsTCTC
ENST00000359842.9:c.49+4887_49+4890delinsTCTC	ENSP00000352900.5:n.49+4887_49+4890delinsTCTC
ENST00000465764.1:n.329-2757_329-2754delinsTCTC
ENST00000619224.1:c.-379+4887_-379+4890delinsTCTC	ENSP00000482458.1:n.-379+4887_-379+4890delinsTCTC
NM_001256570.1:c.-379+4887_-379+4890delinsTCTC	NP_001243499.1:n.-379+4887_-379+4890delinsTCTC
NM_006917.4:c.49+4887_49+4890delinsTCTC	NP_008848.1:n.49+4887_49+4890delinsTCTC
NR_033824.1:n.512-2757_512-2754delinsTCTC
NM_006917.5:c.49+4887_49+4890delinsTCTC MANE Select	NP_008848.1:n.49+4887_49+4890delinsTCTC
NR_033824.2:n.283-2757_283-2754delinsTCTC
NM_001256570.2:c.-379+4887_-379+4890delinsTCTC	NP_001243499.1:n.-379+4887_-379+4890delinsTCTC