Canonical Allele Identifier: CA2692438871

Gene: RXRA

Linked Data

• gnomAD v4: 9-134432131-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134432131C>T , CM000671.2:g.134432131C>T	GRCh38
NC_000009.11:g.137323977C>T , CM000671.1:g.137323977C>T	GRCh37
NC_000009.10:g.136463798C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000481739.2:c.1135+135C>T MANE Select	ENSP00000419692.1:n.1135+135C>T
ENST00000672570.1:c.1054+135C>T	ENSP00000500402.1:n.1054+135C>T
ENST00000356384.4:n.1545+135C>T
ENST00000481739.1:c.1135+135C>T	ENSP00000419692.1:n.1135+135C>T
NM_001291920.1:c.1054+135C>T	NP_001278849.1:n.1054+135C>T
NM_001291921.1:c.844+135C>T	NP_001278850.1:n.844+135C>T
NM_002957.5:c.1135+135C>T	NP_002948.1:n.1135+135C>T
NM_002957.6:c.1135+135C>T MANE Select	NP_002948.1:n.1135+135C>T
NM_001291921.2:c.844+135C>T	NP_001278850.1:n.844+135C>T
NM_001291920.2:c.1054+135C>T	NP_001278849.1:n.1054+135C>T