Canonical Allele Identifier: CA1129841900

Gene: RXRA

Linked Data

• dbSNP Id: rs1831121531
• gnomAD v3: 9-134409964-GGT-G
• gnomAD v4: 9-134409964-GGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134409969_134409970del , CM000671.2:g.134409969_134409970del	GRCh38
NC_000009.11:g.137301815_137301816del , CM000671.1:g.137301815_137301816del	GRCh37
NC_000009.10:g.136441636_136441637del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.610+850_610+851del MANE Select	ENSP00000419692.1:n.610+850_610+851del
ENST00000672570.1:c.529+850_529+851del	ENSP00000500402.1:n.529+850_529+851del
ENST00000356384.4:n.1020+850_1020+851del
ENST00000481739.1:c.610+850_610+851del	ENSP00000419692.1:n.610+850_610+851del
NM_001291920.1:c.529+850_529+851del	NP_001278849.1:n.529+850_529+851del
NM_001291921.1:c.319+850_319+851del	NP_001278850.1:n.319+850_319+851del
NM_002957.5:c.610+850_610+851del	NP_002948.1:n.610+850_610+851del
NM_002957.6:c.610+850_610+851del MANE Select	NP_002948.1:n.610+850_610+851del
NM_001291921.2:c.319+850_319+851del	NP_001278850.1:n.319+850_319+851del
NM_001291920.2:c.529+850_529+851del	NP_001278849.1:n.529+850_529+851del