Canonical Allele Identifier: CA375451980
Gene: RXRA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134408161A>C , CM000671.2:g.134408161A>C GRCh38
NC_000009.11:g.137300007A>C , CM000671.1:g.137300007A>C GRCh37
NC_000009.10:g.136439828A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.292A>C MANE Select ENSP00000419692.1:p.Met98Leu
ENST00000672570.1:c.211A>C ENSP00000500402.1:p.Met71Leu
ENST00000356384.4:n.702A>C
ENST00000481739.1:c.292A>C ENSP00000419692.1:p.Met98Leu
NM_001291920.1:c.211A>C NP_001278849.1:p.Met71Leu
NM_001291921.1:c.1A>C NP_001278850.1:p.Met1Leu
NM_002957.5:c.292A>C NP_002948.1:p.Met98Leu
NM_002957.6:c.292A>C MANE Select NP_002948.1:p.Met98Leu
NM_001291921.2:c.1A>C NP_001278850.1:p.Met1Leu
NM_001291920.2:c.211A>C NP_001278849.1:p.Met71Leu