Canonical Allele Identifier: CA2648887619

Gene: RXRG

Linked Data

• gnomAD v4: 1-165419869-CCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419870_165419871del , CM000663.2:g.165419870_165419871del	GRCh38
NC_000001.10:g.165389107_165389108del , CM000663.1:g.165389107_165389108del	GRCh37
NC_000001.9:g.163655731_163655732del	NCBI36
NG_029517.1:g.30485_30486del
NG_029517.2:g.30485_30486del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.441_442del MANE Select	ENSP00000352900.5:p.Gly148LysfsTer9
ENST00000359842.9:c.441_442del	ENSP00000352900.5:p.Gly148LysfsTer9
ENST00000470566.1:n.366_367del
ENST00000619224.1:c.72_73del	ENSP00000482458.1:p.Gly25LysfsTer9
NM_001256570.1:c.72_73del	NP_001243499.1:p.Gly25LysfsTer9
NM_001256571.1:c.72_73del	NP_001243500.1:p.Gly25LysfsTer9
NM_006917.4:c.441_442del	NP_008848.1:p.Gly148LysfsTer9
NM_006917.5:c.441_442del MANE Select	NP_008848.1:p.Gly148LysfsTer9
NM_001256571.2:c.72_73del	NP_001243500.1:p.Gly25LysfsTer9
NM_001256570.2:c.72_73del	NP_001243499.1:p.Gly25LysfsTer9