Canonical Allele Identifier: CA1204409945

Gene: RXRG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419408_165419417delinsTGAGATGGAG , CM000663.2:g.165419408_165419417delinsTGAGATGGAG	GRCh38
NC_000001.10:g.165388645_165388654delinsTGAGATGGAG , CM000663.1:g.165388645_165388654delinsTGAGATGGAG	GRCh37
NC_000001.9:g.163655269_163655278delinsTGAGATGGAG	NCBI36
NG_029517.1:g.30939_30948delinsCTCCATCTCA
NG_029517.2:g.30939_30948delinsCTCCATCTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.442+453_442+462delinsCTCCATCTCA MANE Select	ENSP00000352900.5:n.442+453_442+462delinsCTCCATCTCA
ENST00000359842.9:c.442+453_442+462delinsCTCCATCTCA	ENSP00000352900.5:n.442+453_442+462delinsCTCCATCTCA
ENST00000470566.1:n.367+453_367+462delinsCTCCATCTCA
ENST00000619224.1:c.73+453_73+462delinsCTCCATCTCA	ENSP00000482458.1:n.73+453_73+462delinsCTCCATCTCA
NM_001256570.1:c.73+453_73+462delinsCTCCATCTCA	NP_001243499.1:n.73+453_73+462delinsCTCCATCTCA
NM_001256571.1:c.73+453_73+462delinsCTCCATCTCA	NP_001243500.1:n.73+453_73+462delinsCTCCATCTCA
NM_006917.4:c.442+453_442+462delinsCTCCATCTCA	NP_008848.1:n.442+453_442+462delinsCTCCATCTCA
NM_006917.5:c.442+453_442+462delinsCTCCATCTCA MANE Select	NP_008848.1:n.442+453_442+462delinsCTCCATCTCA
NM_001256571.2:c.73+453_73+462delinsCTCCATCTCA	NP_001243500.1:n.73+453_73+462delinsCTCCATCTCA
NM_001256570.2:c.73+453_73+462delinsCTCCATCTCA	NP_001243499.1:n.73+453_73+462delinsCTCCATCTCA