Canonical Allele Identifier: CA527077818

Gene: RXRG

Linked Data

• gnomAD v2: 1-165389255-C-CAAAA
• gnomAD v3: 1-165420018-C-CAAAA
• gnomAD v4: 1-165420018-C-CAAAA
• MyVariant Identifiers: chr1:g.165389255_165389256insAAAA (hg19) ; chr1:g.165420018_165420019insAAAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165420020_165420021insAAAA , CM000663.2:g.165420020_165420021insAAAA	GRCh38
NC_000001.10:g.165389257_165389258insAAAA , CM000663.1:g.165389257_165389258insAAAA	GRCh37
NC_000001.9:g.163655881_163655882insAAAA	NCBI36
NG_029517.1:g.30337_30338insTTTT
NG_029517.2:g.30337_30338insTTTT

Transcript Alleles

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