Canonical Allele Identifier: CA1883177684

Gene: RXRA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134409945_134409947delinsGCC , CM000671.2:g.134409945_134409947delinsGCC	GRCh38
NC_000009.11:g.137301791_137301793delinsGCC , CM000671.1:g.137301791_137301793delinsGCC	GRCh37
NC_000009.10:g.136441612_136441614delinsGCC	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000481739.2:c.610+826_610+828delinsGCC MANE Select	ENSP00000419692.1:n.610+826_610+828delinsGCC
ENST00000672570.1:c.529+826_529+828delinsGCC	ENSP00000500402.1:n.529+826_529+828delinsGCC
ENST00000356384.4:n.1020+826_1020+828delinsGCC
ENST00000481739.1:c.610+826_610+828delinsGCC	ENSP00000419692.1:n.610+826_610+828delinsGCC
NM_001291920.1:c.529+826_529+828delinsGCC	NP_001278849.1:n.529+826_529+828delinsGCC
NM_001291921.1:c.319+826_319+828delinsGCC	NP_001278850.1:n.319+826_319+828delinsGCC
NM_002957.5:c.610+826_610+828delinsGCC	NP_002948.1:n.610+826_610+828delinsGCC
NM_002957.6:c.610+826_610+828delinsGCC MANE Select	NP_002948.1:n.610+826_610+828delinsGCC
NM_001291921.2:c.319+826_319+828delinsGCC	NP_001278850.1:n.319+826_319+828delinsGCC
NM_001291920.2:c.529+826_529+828delinsGCC	NP_001278849.1:n.529+826_529+828delinsGCC