Canonical Allele Identifier: CA2648887719

Gene: RXRG

Linked Data

• gnomAD v4: 1-165420110-CTATTTCAAGAAACAGTTTCCAAGTACAGAGTATTTGAAACTGCCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165420111_165420155del , CM000663.2:g.165420111_165420155del	GRCh38
NC_000001.10:g.165389348_165389392del , CM000663.1:g.165389348_165389392del	GRCh37
NC_000001.9:g.163655972_163656016del	NCBI36
NG_029517.1:g.30201_30245del
NG_029517.2:g.30201_30245del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.298-141_298-97del MANE Select	ENSP00000352900.5:n.298-141_298-97del
ENST00000359842.9:c.298-141_298-97del	ENSP00000352900.5:n.298-141_298-97del
ENST00000470566.1:n.223-141_223-97del
ENST00000619224.1:c.-72-141_-72-97del	ENSP00000482458.1:n.-72-141_-72-97del
NM_001256570.1:c.-72-141_-72-97del	NP_001243499.1:n.-72-141_-72-97del
NM_001256571.1:c.-72-141_-72-97del	NP_001243500.1:n.-72-141_-72-97del
NM_006917.4:c.298-141_298-97del	NP_008848.1:n.298-141_298-97del
NM_006917.5:c.298-141_298-97del MANE Select	NP_008848.1:n.298-141_298-97del
NM_001256571.2:c.-72-141_-72-97del	NP_001243500.1:n.-72-141_-72-97del
NM_001256570.2:c.-72-141_-72-97del	NP_001243499.1:n.-72-141_-72-97del