Canonical Allele Identifier: CA1883176831
Gene: RXRA HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134408313G= , CM000671.2:g.134408313G= GRCh38
NC_000009.11:g.137300159G= , CM000671.1:g.137300159G= GRCh37
NC_000009.10:g.136439980G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.430+14G= MANE Select ENSP00000419692.1:n.430+14G=
ENST00000672570.1:c.349+14G= ENSP00000500402.1:n.349+14G=
ENST00000356384.4:n.840+14G=
ENST00000481739.1:c.430+14G= ENSP00000419692.1:n.430+14G=
NM_001291920.1:c.349+14G= NP_001278849.1:n.349+14G=
NM_001291921.1:c.139+14G= NP_001278850.1:n.139+14G=
NM_002957.5:c.430+14G= NP_002948.1:n.430+14G=
NM_002957.6:c.430+14G= MANE Select NP_002948.1:n.430+14G=
NM_001291921.2:c.139+14G= NP_001278850.1:n.139+14G=
NM_001291920.2:c.349+14G= NP_001278849.1:n.349+14G=
Search 100 bp 5'
Search 100 bp 3'