Canonical Allele Identifier: CA2648887570
Gene: RXRG HGNC NCBI

Linked Data

gnomAD v4: 1-165419812-ACAGTGAG-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165419816_165419822del , CM000663.2:g.165419816_165419822del GRCh38
NC_000001.10:g.165389053_165389059del , CM000663.1:g.165389053_165389059del GRCh37
NC_000001.9:g.163655677_163655683del NCBI36
NG_029517.1:g.30537_30543del
NG_029517.2:g.30537_30543del

Transcript Alleles

HGVS Amino-acid change
ENST00000359842.10:c.442+51_442+57del MANE Select ENSP00000352900.5:n.442+51_442+57del
ENST00000359842.9:c.442+51_442+57del ENSP00000352900.5:n.442+51_442+57del
ENST00000470566.1:n.367+51_367+57del
ENST00000619224.1:c.73+51_73+57del ENSP00000482458.1:n.73+51_73+57del
NM_001256570.1:c.73+51_73+57del NP_001243499.1:n.73+51_73+57del
NM_001256571.1:c.73+51_73+57del NP_001243500.1:n.73+51_73+57del
NM_006917.4:c.442+51_442+57del NP_008848.1:n.442+51_442+57del
NM_006917.5:c.442+51_442+57del MANE Select NP_008848.1:n.442+51_442+57del
NM_001256571.2:c.73+51_73+57del NP_001243500.1:n.73+51_73+57del
NM_001256570.2:c.73+51_73+57del NP_001243499.1:n.73+51_73+57del
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