Canonical Allele Identifier: CA1204410226

Gene: RXRG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165420178_165420179delinsAG , CM000663.2:g.165420178_165420179delinsAG	GRCh38
NC_000001.10:g.165389415_165389416delinsAG , CM000663.1:g.165389415_165389416delinsAG	GRCh37
NC_000001.9:g.163656039_163656040delinsAG	NCBI36
NG_029517.1:g.30177_30178delinsCT
NG_029517.2:g.30177_30178delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.298-165_298-164delinsCT MANE Select	ENSP00000352900.5:n.298-165_298-164delinsCT
ENST00000359842.9:c.298-165_298-164delinsCT	ENSP00000352900.5:n.298-165_298-164delinsCT
ENST00000470566.1:n.223-165_223-164delinsCT
ENST00000619224.1:c.-72-165_-72-164delinsCT	ENSP00000482458.1:n.-72-165_-72-164delinsCT
NM_001256570.1:c.-72-165_-72-164delinsCT	NP_001243499.1:n.-72-165_-72-164delinsCT
NM_001256571.1:c.-72-165_-72-164delinsCT	NP_001243500.1:n.-72-165_-72-164delinsCT
NM_006917.4:c.298-165_298-164delinsCT	NP_008848.1:n.298-165_298-164delinsCT
NM_006917.5:c.298-165_298-164delinsCT MANE Select	NP_008848.1:n.298-165_298-164delinsCT
NM_001256571.2:c.-72-165_-72-164delinsCT	NP_001243500.1:n.-72-165_-72-164delinsCT
NM_001256570.2:c.-72-165_-72-164delinsCT	NP_001243499.1:n.-72-165_-72-164delinsCT