Canonical Allele Identifier: CA421572851

Gene: RXRG

Linked Data

• dbSNP Id: rs1439180374
• gnomAD v3: 1-165440005-AG-A
• gnomAD v4: 1-165440005-AG-A
• MyVariant Identifiers: chr1:g.165409243del (hg19) ; chr1:g.165440006del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165440009del , CM000663.2:g.165440009del	GRCh38
NC_000001.10:g.165409246del , CM000663.1:g.165409246del	GRCh37
NC_000001.9:g.163675870del	NCBI36
NG_029517.1:g.10350del
NG_029517.2:g.10350del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.49+4839del MANE Select	ENSP00000352900.5:n.49+4839del
ENST00000359842.9:c.49+4839del	ENSP00000352900.5:n.49+4839del
ENST00000465764.1:n.329-2805del
ENST00000619224.1:c.-379+4839del	ENSP00000482458.1:n.-379+4839del
NM_001256570.1:c.-379+4839del	NP_001243499.1:n.-379+4839del
NM_006917.4:c.49+4839del	NP_008848.1:n.49+4839del
NR_033824.1:n.512-2805del
NM_006917.5:c.49+4839del MANE Select	NP_008848.1:n.49+4839del
NR_033824.2:n.283-2805del
NM_001256570.2:c.-379+4839del	NP_001243499.1:n.-379+4839del