Canonical Allele Identifier: CA2579504521
Gene: RXRA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134408367del , CM000671.2:g.134408367del GRCh38
NC_000009.11:g.137300213del , CM000671.1:g.137300213del GRCh37
NC_000009.10:g.136440034del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.430+68del MANE Select ENSP00000419692.1:n.430+68del
ENST00000672570.1:c.349+68del ENSP00000500402.1:n.349+68del
ENST00000356384.4:n.840+68del
ENST00000481739.1:c.430+68del ENSP00000419692.1:n.430+68del
NM_001291920.1:c.349+68del NP_001278849.1:n.349+68del
NM_001291921.1:c.139+68del NP_001278850.1:n.139+68del
NM_002957.5:c.430+68del NP_002948.1:n.430+68del
NM_002957.6:c.430+68del MANE Select NP_002948.1:n.430+68del
NM_001291921.2:c.139+68del NP_001278850.1:n.139+68del
NM_001291920.2:c.349+68del NP_001278849.1:n.349+68del