Canonical Allele Identifier: CA32223410

Gene: RXRG

Linked Data

• dbSNP Id: rs35145392
• MyVariant Identifiers: chr1:g.165409094del (hg19) ; chr1:g.165439857del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165439858del , CM000663.2:g.165439858del	GRCh38
NC_000001.10:g.165409095del , CM000663.1:g.165409095del	GRCh37
NC_000001.9:g.163675719del	NCBI36
NG_029517.1:g.10499del
NG_029517.2:g.10499del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.49+4988del MANE Select	ENSP00000352900.5:n.49+4988del
ENST00000359842.9:c.49+4988del	ENSP00000352900.5:n.49+4988del
ENST00000465764.1:n.329-2656del
ENST00000619224.1:c.-379+4988del	ENSP00000482458.1:n.-379+4988del
NM_001256570.1:c.-379+4988del	NP_001243499.1:n.-379+4988del
NM_006917.4:c.49+4988del	NP_008848.1:n.49+4988del
NR_033824.1:n.512-2656del
NM_006917.5:c.49+4988del MANE Select	NP_008848.1:n.49+4988del
NR_033824.2:n.283-2656del
NM_001256570.2:c.-379+4988del	NP_001243499.1:n.-379+4988del