Canonical Allele Identifier: CA1883184541
Gene: RXRA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134429310A= , CM000671.2:g.134429310A= GRCh38
NC_000009.11:g.137321156A= , CM000671.1:g.137321156A= GRCh37
NC_000009.10:g.136460977A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_002957.6:c.1043+70A= MANE Select NP_002948.1:n.1043+70A=
ENST00000481739.2:c.1043+70A= MANE Select ENSP00000419692.1:n.1043+70A=
NM_001291920.1:c.962+70A= NP_001278849.1:n.962+70A=
NM_001291920.2:c.962+70A= NP_001278849.1:n.962+70A=
NM_001291921.1:c.752+70A= NP_001278850.1:n.752+70A=
NM_001291921.2:c.752+70A= NP_001278850.1:n.752+70A=
NM_002957.5:c.1043+70A= NP_002948.1:n.1043+70A=
ENST00000356384.4:n.1453+70A=
ENST00000481739.1:c.1043+70A= ENSP00000419692.1:n.1043+70A=
ENST00000672570.1:c.962+70A= ENSP00000500402.1:n.962+70A=