Canonical Allele Identifier: CA890586043

Gene: RXRG

Linked Data

• dbSNP Id: rs1283534428
• gnomAD v3: 1-165419461-GC-G
• gnomAD v4: 1-165419461-GC-G
• MyVariant Identifiers: chr1:g.165388699del (hg19) ; chr1:g.165419462del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419462del , CM000663.2:g.165419462del	GRCh38
NC_000001.10:g.165388699del , CM000663.1:g.165388699del	GRCh37
NC_000001.9:g.163655323del	NCBI36
NG_029517.1:g.30894del
NG_029517.2:g.30894del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.442+408del MANE Select	ENSP00000352900.5:n.442+408del
ENST00000359842.9:c.442+408del	ENSP00000352900.5:n.442+408del
ENST00000470566.1:n.367+408del
ENST00000619224.1:c.73+408del	ENSP00000482458.1:n.73+408del
NM_001256570.1:c.73+408del	NP_001243499.1:n.73+408del
NM_001256571.1:c.73+408del	NP_001243500.1:n.73+408del
NM_006917.4:c.442+408del	NP_008848.1:n.442+408del
NM_006917.5:c.442+408del MANE Select	NP_008848.1:n.442+408del
NM_001256571.2:c.73+408del	NP_001243500.1:n.73+408del
NM_001256570.2:c.73+408del	NP_001243499.1:n.73+408del