Canonical Allele Identifier: CA527077798

Gene: RXRG

Linked Data

• dbSNP Id: rs1363024282
• gnomAD v2: 1-165388654-G-GTTTTTTTTT
• gnomAD v3: 1-165419417-G-GTTTTTTTTT
• gnomAD v4: 1-165419417-G-GTTTTTTTTT
• MyVariant Identifiers: chr1:g.165388654_165388655insTTTTTTTTT (hg19) ; chr1:g.165419417_165419418insTTTTTTTTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419418_165419419insTTTTTTTTT , CM000663.2:g.165419418_165419419insTTTTTTTTT	GRCh38
NC_000001.10:g.165388655_165388656insTTTTTTTTT , CM000663.1:g.165388655_165388656insTTTTTTTTT	GRCh37
NC_000001.9:g.163655279_163655280insTTTTTTTTT	NCBI36
NG_029517.1:g.30938_30939insAAAAAAAAA
NG_029517.2:g.30938_30939insAAAAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.442+452_442+453insAAAAAAAAA MANE Select	ENSP00000352900.5:n.442+452_442+453insAAAAAAAAA
ENST00000359842.9:c.442+452_442+453insAAAAAAAAA	ENSP00000352900.5:n.442+452_442+453insAAAAAAAAA
ENST00000470566.1:n.367+452_367+453insAAAAAAAAA
ENST00000619224.1:c.73+452_73+453insAAAAAAAAA	ENSP00000482458.1:n.73+452_73+453insAAAAAAAAA
NM_001256570.1:c.73+452_73+453insAAAAAAAAA	NP_001243499.1:n.73+452_73+453insAAAAAAAAA
NM_001256571.1:c.73+452_73+453insAAAAAAAAA	NP_001243500.1:n.73+452_73+453insAAAAAAAAA
NM_006917.4:c.442+452_442+453insAAAAAAAAA	NP_008848.1:n.442+452_442+453insAAAAAAAAA
NM_006917.5:c.442+452_442+453insAAAAAAAAA MANE Select	NP_008848.1:n.442+452_442+453insAAAAAAAAA
NM_001256571.2:c.73+452_73+453insAAAAAAAAA	NP_001243500.1:n.73+452_73+453insAAAAAAAAA
NM_001256570.2:c.73+452_73+453insAAAAAAAAA	NP_001243499.1:n.73+452_73+453insAAAAAAAAA