Canonical Allele Identifier: CA1883176786
Gene: RXRA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134408200_134408201delinsCT , CM000671.2:g.134408200_134408201delinsCT GRCh38
NC_000009.11:g.137300046_137300047delinsCT , CM000671.1:g.137300046_137300047delinsCT GRCh37
NC_000009.10:g.136439867_136439868delinsCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.331_332delinsCT MANE Select ENSP00000419692.1:p.Leu111=
ENST00000672570.1:c.250_251delinsCT ENSP00000500402.1:p.Leu84=
ENST00000356384.4:n.741_742delinsCT
ENST00000481739.1:c.331_332delinsCT ENSP00000419692.1:p.Leu111=
NM_001291920.1:c.250_251delinsCT NP_001278849.1:p.Leu84=
NM_001291921.1:c.40_41delinsCT NP_001278850.1:p.Leu14=
NM_002957.5:c.331_332delinsCT NP_002948.1:p.Leu111=
NM_002957.6:c.331_332delinsCT MANE Select NP_002948.1:p.Leu111=
NM_001291921.2:c.40_41delinsCT NP_001278850.1:p.Leu14=
NM_001291920.2:c.250_251delinsCT NP_001278849.1:p.Leu84=