Canonical Allele Identifier: CA2692438875

Gene: RXRA

Linked Data

• gnomAD v4: 9-134432133-C-CCCTCCCAGTG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134432134_134432143dup , CM000671.2:g.134432134_134432143dup	GRCh38
NC_000009.11:g.137323980_137323989dup , CM000671.1:g.137323980_137323989dup	GRCh37
NC_000009.10:g.136463801_136463810dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000481739.2:c.1135+138_1135+147dup MANE Select	ENSP00000419692.1:n.1135+138_1135+147dup
ENST00000672570.1:c.1054+138_1054+147dup	ENSP00000500402.1:n.1054+138_1054+147dup
ENST00000356384.4:n.1545+138_1545+147dup
ENST00000481739.1:c.1135+138_1135+147dup	ENSP00000419692.1:n.1135+138_1135+147dup
NM_001291920.1:c.1054+138_1054+147dup	NP_001278849.1:n.1054+138_1054+147dup
NM_001291921.1:c.844+138_844+147dup	NP_001278850.1:n.844+138_844+147dup
NM_002957.5:c.1135+138_1135+147dup	NP_002948.1:n.1135+138_1135+147dup
NM_002957.6:c.1135+138_1135+147dup MANE Select	NP_002948.1:n.1135+138_1135+147dup
NM_001291921.2:c.844+138_844+147dup	NP_001278850.1:n.844+138_844+147dup
NM_001291920.2:c.1054+138_1054+147dup	NP_001278849.1:n.1054+138_1054+147dup