Canonical Allele Identifier: CA1883176788
Gene: RXRA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134408202G= , CM000671.2:g.134408202G= GRCh38
NC_000009.11:g.137300048G= , CM000671.1:g.137300048G= GRCh37
NC_000009.10:g.136439869G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.333G= MANE Select ENSP00000419692.1:p.Leu111=
ENST00000672570.1:c.252G= ENSP00000500402.1:p.Leu84=
ENST00000356384.4:n.743G=
ENST00000481739.1:c.333G= ENSP00000419692.1:p.Leu111=
NM_001291920.1:c.252G= NP_001278849.1:p.Leu84=
NM_001291921.1:c.42G= NP_001278850.1:p.Leu14=
NM_002957.5:c.333G= NP_002948.1:p.Leu111=
NM_002957.6:c.333G= MANE Select NP_002948.1:p.Leu111=
NM_001291921.2:c.42G= NP_001278850.1:p.Leu14=
NM_001291920.2:c.252G= NP_001278849.1:p.Leu84=