Canonical Allele Identifier: CA1883168531
Community Standard Title: NM_002957.6(RXRA):c.611-542A=
Gene: RXRA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134416616A= , CM000671.2:g.134416616A= GRCh38
NC_000009.11:g.137308462A= , CM000671.1:g.137308462A= GRCh37
NC_000009.10:g.136448283A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_002957.6:c.611-542A= MANE Select NP_002948.1:n.611-542A=
ENST00000481739.2:c.611-542A= MANE Select ENSP00000419692.1:n.611-542A=
NM_001291920.1:c.530-542A= NP_001278849.1:n.530-542A=
NM_001291920.2:c.530-542A= NP_001278849.1:n.530-542A=
NM_001291921.1:c.320-542A= NP_001278850.1:n.320-542A=
NM_001291921.2:c.320-542A= NP_001278850.1:n.320-542A=
NM_002957.5:c.611-542A= NP_002948.1:n.611-542A=
ENST00000356384.4:n.1021-542A=
ENST00000481739.1:c.611-542A= ENSP00000419692.1:n.611-542A=
ENST00000672570.1:c.530-542A= ENSP00000500402.1:n.530-542A=