Canonical Allele Identifier: CA860856599

Gene: RXRA

Linked Data

• dbSNP Id: rs1355952191
• gnomAD v4: 9-134408312-TG-T
• MyVariant Identifiers: chr9:g.137300159del (hg19) ; chr9:g.134408313del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408317del , CM000671.2:g.134408317del	GRCh38
NC_000009.11:g.137300163del , CM000671.1:g.137300163del	GRCh37
NC_000009.10:g.136439984del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.430+18del MANE Select	ENSP00000419692.1:n.430+18del
ENST00000672570.1:c.349+18del	ENSP00000500402.1:n.349+18del
ENST00000356384.4:n.840+18del
ENST00000481739.1:c.430+18del	ENSP00000419692.1:n.430+18del
NM_001291920.1:c.349+18del	NP_001278849.1:n.349+18del
NM_001291921.1:c.139+18del	NP_001278850.1:n.139+18del
NM_002957.5:c.430+18del	NP_002948.1:n.430+18del
NM_002957.6:c.430+18del MANE Select	NP_002948.1:n.430+18del
NM_001291921.2:c.139+18del	NP_001278850.1:n.139+18del
NM_001291920.2:c.349+18del	NP_001278849.1:n.349+18del