Canonical Allele Identifier: CA1883177685
Gene: RXRA HGNC NCBI

Linked Data

dbSNP Id: rs1831121129
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134409947_134409948del , CM000671.2:g.134409947_134409948del GRCh38
NC_000009.11:g.137301793_137301794del , CM000671.1:g.137301793_137301794del GRCh37
NC_000009.10:g.136441614_136441615del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000481739.2:c.610+828_610+829del MANE Select ENSP00000419692.1:n.610+828_610+829del
ENST00000672570.1:c.529+828_529+829del ENSP00000500402.1:n.529+828_529+829del
ENST00000356384.4:n.1020+828_1020+829del
ENST00000481739.1:c.610+828_610+829del ENSP00000419692.1:n.610+828_610+829del
NM_001291920.1:c.529+828_529+829del NP_001278849.1:n.529+828_529+829del
NM_001291921.1:c.319+828_319+829del NP_001278850.1:n.319+828_319+829del
NM_002957.5:c.610+828_610+829del NP_002948.1:n.610+828_610+829del
NM_002957.6:c.610+828_610+829del MANE Select NP_002948.1:n.610+828_610+829del
NM_001291921.2:c.319+828_319+829del NP_001278850.1:n.319+828_319+829del
NM_001291920.2:c.529+828_529+829del NP_001278849.1:n.529+828_529+829del
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