Canonical Allele Identifier: CA2692437232

Gene: RXRA

Linked Data

• gnomAD v4: 9-134408302-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408302A>G , CM000671.2:g.134408302A>G	GRCh38
NC_000009.11:g.137300148A>G , CM000671.1:g.137300148A>G	GRCh37
NC_000009.10:g.136439969A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.430+3A>G MANE Select	ENSP00000419692.1:n.430+3A>G
ENST00000672570.1:c.349+3A>G	ENSP00000500402.1:n.349+3A>G
ENST00000356384.4:n.840+3A>G
ENST00000481739.1:c.430+3A>G	ENSP00000419692.1:n.430+3A>G
NM_001291920.1:c.349+3A>G	NP_001278849.1:n.349+3A>G
NM_001291921.1:c.139+3A>G	NP_001278850.1:n.139+3A>G
NM_002957.5:c.430+3A>G	NP_002948.1:n.430+3A>G
NM_002957.6:c.430+3A>G MANE Select	NP_002948.1:n.430+3A>G
NM_001291921.2:c.139+3A>G	NP_001278850.1:n.139+3A>G
NM_001291920.2:c.349+3A>G	NP_001278849.1:n.349+3A>G