Canonical Allele Identifier: CA2692437264

Gene: RXRA

Linked Data

• gnomAD v4: 9-134408355-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408355G>C , CM000671.2:g.134408355G>C	GRCh38
NC_000009.11:g.137300201G>C , CM000671.1:g.137300201G>C	GRCh37
NC_000009.10:g.136440022G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.430+56G>C MANE Select	ENSP00000419692.1:n.430+56G>C
ENST00000672570.1:c.349+56G>C	ENSP00000500402.1:n.349+56G>C
ENST00000356384.4:n.840+56G>C
ENST00000481739.1:c.430+56G>C	ENSP00000419692.1:n.430+56G>C
NM_001291920.1:c.349+56G>C	NP_001278849.1:n.349+56G>C
NM_001291921.1:c.139+56G>C	NP_001278850.1:n.139+56G>C
NM_002957.5:c.430+56G>C	NP_002948.1:n.430+56G>C
NM_002957.6:c.430+56G>C MANE Select	NP_002948.1:n.430+56G>C
NM_001291921.2:c.139+56G>C	NP_001278850.1:n.139+56G>C
NM_001291920.2:c.349+56G>C	NP_001278849.1:n.349+56G>C